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Tytuł :
Porencephaly in an Italian neonate with foetal alcohol spectrum disorder: A case report.
Autorzy :
Mencarelli A; Pediatric Clinic, Department of Medical and Surgical Sciences, Università degli Studi di Perugia.
Prontera P; Medical Genetics Unit, Santa Maria della Misericordia Hospital.
Stangoni G; Medical Genetics Unit, Santa Maria della Misericordia Hospital.
Troiani S; Neonatology Unit, Santa Maria della Misericordia Hospital, Perugia.
Becchetti T; Neonatology Unit, Santa Maria della Misericordia Hospital, Perugia.
Pacitto A; Pediatric Clinic, Department of Medical and Surgical Sciences, Università degli Studi di Perugia.
Esposito S; Pediatric Clinic, Pietro Barilla Children's Hospital, Department of Medicine and Surgery, University of Parma, Parma, Italy.
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Źródło :
Medicine [Medicine (Baltimore)] 2020 Jul 31; Vol. 99 (31), pp. e21384.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Fetal Alcohol Spectrum Disorders/*diagnosis
Porencephaly/*diagnosis
Female ; Glucuronates/analysis ; Hair/chemistry ; Humans ; Infant, Newborn ; Italy ; Male ; Porencephaly/complications ; Pregnancy
Czasopismo naukowe
Tytuł :
Vasospasm Following Hemispherectomy: A Case Report of a Novel Complication.
Autorzy :
Morsi A; Department of Neurosurgery, Cleveland Clinic Foundation, Cleveland, Ohio, USA. Electronic address: .
Maldonado A; Department of Neurosurgery, University of Illinois College of Medicine Peoria, Peoria, Illinois, USA.
Lal D; Genomic Medicine Institute, Cleveland Clinic Foundation, Cleveland, Ohio, USA.
Moosa ANV; Department of Neurology, Cleveland Clinic Foundation, Cleveland, Ohio, USA.
Pestana-Knight E; Department of Neurology, Cleveland Clinic Foundation, Cleveland, Ohio, USA.
Bingaman W; Department of Neurosurgery, Cleveland Clinic Foundation, Cleveland, Ohio, USA.
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Źródło :
World neurosurgery [World Neurosurg] 2020 May; Vol. 137, pp. 357-361. Date of Electronic Publication: 2020 Feb 12.
Typ publikacji :
Case Reports
MeSH Terms :
Hemispherectomy*
Brain Ischemia/*diagnostic imaging
Collagen Type IV/*genetics
Drug Resistant Epilepsy/*surgery
Epilepsies, Partial/*surgery
Porencephaly/*genetics
Postoperative Complications/*diagnostic imaging
Vasospasm, Intracranial/*diagnostic imaging
Adolescent ; Angiography, Digital Subtraction ; Brain Ischemia/physiopathology ; Brain Ischemia/therapy ; Cerebral Angiography ; Developmental Disabilities/complications ; Drug Resistant Epilepsy/complications ; Drug Resistant Epilepsy/diagnostic imaging ; Drug Resistant Epilepsy/physiopathology ; Epilepsies, Partial/complications ; Epilepsies, Partial/diagnostic imaging ; Epilepsies, Partial/physiopathology ; Fatal Outcome ; Hemianopsia/complications ; Hemiplegia/complications ; Humans ; Male ; Porencephaly/complications ; Postoperative Complications/physiopathology ; Postoperative Complications/therapy ; Vasospasm, Intracranial/physiopathology ; Vasospasm, Intracranial/therapy
Raport
Tytuł :
COL4A1 MUTATIONS IN TWO INFANTS WITH CONGENITAL CATARACTS AND PORENCEPHALY: AN OPHTHALMOLOGIC PERSPECTIVE.
Autorzy :
Khan AO; Eye Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates.
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Źródło :
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus [J AAPOS] 2019 Dec; Vol. 23 (6), pp. 362. Date of Electronic Publication: 2019 Sep 13.
Typ publikacji :
Letter; Comment
MeSH Terms :
Brain Diseases*
Cataract*
Porencephaly*
Collagen Type IV ; Humans ; Infant ; Mutation
Opinia redakcyjna
Tytuł :
Reply.
Autorzy :
Nau SA; Department of Ophthalmology, University of Colorado, Aurora, Colorado.
McCourt EA; Department of Ophthalmology, University of Colorado, Aurora, Colorado.
Jung JL; Department of Ophthalmology, University of Colorado, Aurora, Colorado.
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Źródło :
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus [J AAPOS] 2019 Dec; Vol. 23 (6), pp. 362. Date of Electronic Publication: 2019 Sep 30.
Typ publikacji :
Letter; Comment
MeSH Terms :
Cataract*
Ophthalmology*
Porencephaly*
Collagen Type IV ; Humans ; Infant ; Mutation
Opinia redakcyjna
Tytuł :
Asymmetry of the bilateral bispectral index in a hemiparetic patient with porencephaly.
Autorzy :
Kira S; Division of Anesthesia, Medical Department, Beppu Developmental Medicine & Rehabilitation Center, 4075-1 Tsurumi, Beppu, Oita 874-0838, Japan. Electronic address: .
Shiihara K; Department of Anesthesiology and Intensive Care Medicine, Oita University Faculty of Medicine, 1-1 Idaigaoka, Hasama-machi, Yufu, Oita 879-5593, Japan. Electronic address: .
Okuda K; Department of Anesthesiology and Intensive Care Medicine, Oita University Faculty of Medicine, 1-1 Idaigaoka, Hasama-machi, Yufu, Oita 879-5593, Japan. Electronic address: .
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Źródło :
Journal of clinical anesthesia [J Clin Anesth] 2019 Aug; Vol. 55, pp. 31-32. Date of Electronic Publication: 2018 Dec 26.
Typ publikacji :
Case Reports; Letter
MeSH Terms :
Consciousness Monitors*
Monitoring, Intraoperative/*methods
Orthopedic Procedures/*adverse effects
Porencephaly/*complications
Adolescent ; Anesthesia, General/adverse effects ; Anesthesia, General/methods ; Consciousness/physiology ; Electroencephalography ; Female ; Humans ; Lower Extremity/surgery ; Monitoring, Intraoperative/instrumentation ; Paresis/complications ; Porencephaly/physiopathology
Raport
Tytuł :
COL4A1 mutations in two infants with congenital cataracts and porencephaly: an ophthalmologic perspective.
Autorzy :
Nau S; Department of Ophthalmology, University of Colorado School of Medicine, Aurora, Colorado.
McCourt EA; Department of Ophthalmology, University of Colorado School of Medicine, Aurora, Colorado.
Maloney JA; Department of Radiology, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, Colorado.
Van Hove JL; Section of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado.
Saenz M; Section of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado.
Jung JL; Department of Ophthalmology, University of Colorado School of Medicine, Aurora, Colorado. Electronic address: .
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Źródło :
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus [J AAPOS] 2019 Aug; Vol. 23 (4), pp. 246-248. Date of Electronic Publication: 2019 May 22.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Abnormalities, Multiple*
Mutation*
Cataract/*genetics
Collagen Type IV/*genetics
DNA/*genetics
Porencephaly/*genetics
Brain/diagnostic imaging ; Cataract/congenital ; Cataract/diagnosis ; Collagen Type IV/metabolism ; DNA Mutational Analysis ; Female ; Humans ; Infant ; Magnetic Resonance Imaging/methods ; Male ; Pedigree ; Phenotype ; Porencephaly/diagnosis
Czasopismo naukowe
Tytuł :
Further refinement of COL4A1 and COL4A2 related cortical malformations.
Autorzy :
Cavallin M; Paris Descartes - Sorbonne Paris Cité University, Imagine Institute, Paris, France; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR 1163, Imagine Institute, Paris, France.
Mine M; AP-HP, Groupe Hospitalier Saint-Louis Lariboisière-Fernand-Widal, Service de Génétique Moléculaire Neurovasculaire, Centre de Reference des Maladies Vasculaires Rares du Cerveau et de l'Oeil (CERVCO), Paris, France; INSERM UMR 1161, Génétique et Physiopathologie des Maladies Cérébro-vasculaires, Paris, France.
Philbert M; Paris Descartes - Sorbonne Paris Cité University, Imagine Institute, Paris, France; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR 1163, Imagine Institute, Paris, France.
Boddaert N; Pediatric Radiology, Necker Enfants Malades University Hospital, APHP, Paris, France; Image - Institut Imagine, INSERM UMR 1163, Université Paris Descartes, Hôpital Necker Enfants Malades, Paris, France.
Lepage JM; Service de Neuropédiatrie CHU Rennes, France.
Coste T; AP-HP, Groupe Hospitalier Saint-Louis Lariboisière-Fernand-Widal, Service de Génétique Moléculaire Neurovasculaire, Centre de Reference des Maladies Vasculaires Rares du Cerveau et de l'Oeil (CERVCO), Paris, France; INSERM UMR 1161, Génétique et Physiopathologie des Maladies Cérébro-vasculaires, Paris, France.
Lopez-Gonzalez V; Sección de Genética Médica y Dismorfología, Servicio de Pediatría, Hospital Clínico Universitario Virgen de la Arrixaca, IMIB-Arrixaca, Murcia, Spain.
Sanchez-Soler MJ; Sección de Genética Médica y Dismorfología, Servicio de Pediatría, Hospital Clínico Universitario Virgen de la Arrixaca, IMIB-Arrixaca, Murcia, Spain.
Ballesta-Martínez MJ; Sección de Genética Médica y Dismorfología, Servicio de Pediatría, Hospital Clínico Universitario Virgen de la Arrixaca, IMIB-Arrixaca, Murcia, Spain.
Remerand G; Service de Néonatologie, CHU Estaing, Clermont-ferrand, France.
Pasquier L; Service de Génétique CHU Rennes, France.
Guët A; Néonatologie et Pédiatrie, Hôpital Louis-Mourier, Colombes, France.
Chelly J; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France; CNRS U7104, Illkirch, France; INSERM U964, Illkirch, France; Université de Strasbourg, Illkirch, France; Service de Diagnostic Génétique, Hôpital Civil de Strasbourg, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Lascelles K; Department of Neuroscience, Evelina London Children's Hospital, St Thomas' Hospital, Westminster Bridge Road, London SE1 7EH, UK.
Prieto-Morin C; AP-HP, Groupe Hospitalier Saint-Louis Lariboisière-Fernand-Widal, Service de Génétique Moléculaire Neurovasculaire, Centre de Reference des Maladies Vasculaires Rares du Cerveau et de l'Oeil (CERVCO), Paris, France; INSERM UMR 1161, Génétique et Physiopathologie des Maladies Cérébro-vasculaires, Paris, France.
Kossorotoff M; Pediatric Neurology, APHP- Necker Enfants Malades Hospital, Paris, France; French Centre for Paediatric Stroke, AP-HP, Necker Enfants Malades, 75015, Paris, France.
Tournier Lasserve E; AP-HP, Groupe Hospitalier Saint-Louis Lariboisière-Fernand-Widal, Service de Génétique Moléculaire Neurovasculaire, Centre de Reference des Maladies Vasculaires Rares du Cerveau et de l'Oeil (CERVCO), Paris, France; INSERM UMR 1161, Génétique et Physiopathologie des Maladies Cérébro-vasculaires, Paris, France.
Bahi-Buisson N; Paris Descartes - Sorbonne Paris Cité University, Imagine Institute, Paris, France; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR 1163, Imagine Institute, Paris, France; Pediatric Neurology, APHP- Necker Enfants Malades Hospital, Paris, France; National Rare Disease Center- Centre de Référence 'Déficiences Intellectuelles de Causes Rares', AP-HP, Necker Enfants Malades, 75015, Paris, France. Electronic address: .
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Źródło :
European journal of medical genetics [Eur J Med Genet] 2018 Dec; Vol. 61 (12), pp. 765-772. Date of Electronic Publication: 2018 Oct 11.
Typ publikacji :
Journal Article
MeSH Terms :
Collagen Type IV/*genetics
Polymicrogyria/*genetics
Porencephaly/*genetics
Schizencephaly/*genetics
Child ; Child, Preschool ; Female ; Humans ; Infant ; Magnetic Resonance Imaging ; Male ; Mutation ; Polymicrogyria/diagnostic imaging ; Polymicrogyria/physiopathology ; Porencephaly/diagnostic imaging ; Porencephaly/physiopathology ; Schizencephaly/diagnostic imaging ; Schizencephaly/physiopathology
Czasopismo naukowe
Tytuł :
A case of tubulinopathy presenting with porencephaly caused by a novel missense mutation in the TUBA1A gene.
Autorzy :
Sato T; Department of Pediatrics, Nagasaki University Hospital, Japan. Electronic address: .
Kato M; Department of Pediatrics, Showa University School of Medicine, Japan.
Moriyama K; Department of Pediatrics, Nagasaki University Hospital, Japan.
Haraguchi K; Department of Pediatrics, Nagasaki University Hospital, Japan.
Saitsu H; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Japan.
Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Japan.
Moriuchi H; Department of Pediatrics, Nagasaki University Hospital, Japan.
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Źródło :
Brain & development [Brain Dev] 2018 Oct; Vol. 40 (9), pp. 819-823. Date of Electronic Publication: 2018 Jun 12.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Mutation, Missense*
Porencephaly/*genetics
Proteostasis Deficiencies/*genetics
Tubulin/*genetics
Female ; Humans ; Infant ; Phenotype ; Porencephaly/diagnostic imaging ; Porencephaly/drug therapy ; Porencephaly/physiopathology ; Proteostasis Deficiencies/diagnostic imaging ; Proteostasis Deficiencies/drug therapy ; Proteostasis Deficiencies/physiopathology
Czasopismo naukowe
Tytuł :
MEG May Reveal Hidden Population of Spikes in Epilepsy With Porencephalic Cyst/Encephalomalacia.
Autorzy :
Kakisaka Y; Epilepsy Center, Department of Neurology, Cleveland Clinic, Cleveland, Ohio, U.S.A.; and †Department of Epileptology, Tohoku University School of Medicine, Sendai, Japan.
Wang ZI
Shibata S
Takahashi Y
Mosher JC
Alexopoulos AV
Burgess RC
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Źródło :
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society [J Clin Neurophysiol] 2017 Nov; Vol. 34 (6), pp. 546-549.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Magnetoencephalography*
Brain/*physiopathology
Encephalomalacia/*diagnosis
Epilepsy/*diagnosis
Porencephaly/*diagnosis
Electroencephalography ; Encephalomalacia/complications ; Encephalomalacia/physiopathology ; Epilepsy/complications ; Epilepsy/physiopathology ; Female ; Humans ; Male ; Middle Aged ; Porencephaly/complications ; Porencephaly/physiopathology ; Young Adult
Czasopismo naukowe
Tytuł :
Novel COL4A2 variant in a large pedigree: Consequences and dilemmas.
Autorzy :
McGovern M; Department of Paediatrics, National University of Ireland Galway & Galway University Hospital, Galway, Ireland.
Flanagan O; Department of Paediatrics, National University of Ireland Galway & Galway University Hospital, Galway, Ireland.
Lynch B; Department of Paediatric Neurology, Temple Street Children's University Hospital, Dublin, Ireland.
Lynch SA; Department of Clinical Genetics, Our Lady's Children's Hospital, Dublin, Ireland.
Allen NM; Department of Paediatrics, National University of Ireland Galway & Galway University Hospital, Galway, Ireland.
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Źródło :
Clinical genetics [Clin Genet] 2017 Oct; Vol. 92 (4), pp. 447-448. Date of Electronic Publication: 2017 May 25.
Typ publikacji :
Letter
MeSH Terms :
Arthritis, Juvenile/*genetics
Collagen/*metabolism
Collagen Type IV/*genetics
Porencephaly/*genetics
Arthritis, Juvenile/complications ; Arthritis, Juvenile/physiopathology ; Bone Diseases, Developmental ; Brain/metabolism ; Brain/physiopathology ; Collagen/biosynthesis ; Collagen/genetics ; Craniofacial Abnormalities ; Female ; Heterozygote ; Humans ; Hyperostosis ; Hypertelorism ; Male ; Mutation ; Pedigree ; Phenotype ; Porencephaly/complications ; Porencephaly/physiopathology
SCR Disease Name :
Schwartz-Lelek syndrome
Opinia redakcyjna
Tytuł :
Life-threatening muscle complications of COL4A1-related disorder.
Autorzy :
Okano S; Department of Pediatrics, Asahikawa Medical University, Japan. Electronic address: .
Shimada S; Department of Pediatrics, Asahikawa Medical University, Japan.
Tanaka R; Department of Pediatrics, Asahikawa Medical University, Japan.
Okayama A; Department of Pediatrics, Asahikawa Medical University, Japan.
Kajihama A; Department of Pediatrics, Asahikawa Medical University, Japan.
Suzuki N; Department of Pediatrics, Asahikawa Medical University, Japan.
Nakau K; Department of Pediatrics, Asahikawa Medical University, Japan.
Takahashi S; Department of Pediatrics, Asahikawa Medical University, Japan.
Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Japan.
Saitsu H; Department of Biochemistry, Hamamatsu University School of Medicine, Japan.
Tanboon J; Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Japan.
Nishino I; Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Japan; Departments of Genome Medicine Development and Clinical Genome Analysis, Medical Genome Center (MGC), NCNP, Japan.
Azuma H; Department of Pediatrics, Asahikawa Medical University, Japan.
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Źródło :
Brain & development [Brain Dev] 2020 Jan; Vol. 42 (1), pp. 93-97. Date of Electronic Publication: 2019 Sep 18.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Cardiomyopathy, Hypertrophic/*genetics
Collagen Type IV/*genetics
Muscle, Skeletal/*pathology
Porencephaly/*genetics
Rhabdomyolysis/*genetics
Child, Preschool ; Humans ; Male ; Mutation
Czasopismo naukowe
Tytuł :
Normal immunofluorescence pattern of skin basement membranes in a family with porencephaly due to COL4A1 G749S mutation.
Autorzy :
Gasparini S; Department of Medical and Surgical Sciences, Magna Graecia University, Catanzaro, Italy.; Regional Epilepsy Center, Bianchi-Melacrino-Morelli Hospital, Reggio Calabria, Italy.
Qualtieri A; Institute of Neurological Sciences, National Research Council, Cosenza, Italy.
Ferlazzo E; Department of Medical and Surgical Sciences, Magna Graecia University, Catanzaro, Italy.; Regional Epilepsy Center, Bianchi-Melacrino-Morelli Hospital, Reggio Calabria, Italy.
Cianci V; Regional Epilepsy Center, Bianchi-Melacrino-Morelli Hospital, Reggio Calabria, Italy.
Patitucci A; Institute of Neurological Sciences, National Research Council, Cosenza, Italy.
Spadafora P; Institute of Neurological Sciences, National Research Council, Cosenza, Italy.
Aguglia U; Department of Medical and Surgical Sciences, Magna Graecia University, Catanzaro, Italy. .; Regional Epilepsy Center, Bianchi-Melacrino-Morelli Hospital, Reggio Calabria, Italy. .
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Źródło :
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2016 Mar; Vol. 37 (3), pp. 459-63. Date of Electronic Publication: 2015 Dec 19.
Typ publikacji :
Journal Article
MeSH Terms :
Mutation*
Basement Membrane/*pathology
Collagen Type IV/*metabolism
Porencephaly/*genetics
Porencephaly/*pathology
Adult ; Basement Membrane/blood supply ; Basement Membrane/innervation ; Basement Membrane/metabolism ; Collagen Type IV/genetics ; Family ; Female ; Fluorescent Antibody Technique ; Humans ; Male ; Microscopy, Confocal ; Middle Aged ; Porencephaly/metabolism ; Sebaceous Glands/metabolism ; Sebaceous Glands/pathology ; Young Adult
Czasopismo naukowe
Tytuł :
A case of left congenital homonymous hemianopia associated with right occipital porencephaly.
Autorzy :
Han S; McMaster University, Hamilton, Ont.
Albreiki D; University of Ottawa Eye Institute, Ottawa, Ont.. Electronic address: .
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Źródło :
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie [Can J Ophthalmol] 2019 Oct; Vol. 54 (5), pp. e244-e246. Date of Electronic Publication: 2019 Apr 02.
Typ publikacji :
Case Reports; Letter
MeSH Terms :
Abnormalities, Multiple*
Visual Acuity*
Hemianopsia/*congenital
Occipital Lobe/*diagnostic imaging
Porencephaly/*diagnosis
Visual Fields/*physiology
Female ; Hemianopsia/diagnosis ; Humans ; Magnetic Resonance Imaging ; Middle Aged ; Tomography, Optical Coherence
Raport
Tytuł :
Evaluation of long-term neurodevelopment in twin-twin transfusion syndrome after laser therapy.
Autorzy :
Sananès N; Department of Obstetrics and Gynecology, Strasbourg University Hospital, Strasbourg, France.; INSERM, UMR-S 1121, 'Biomatériaux et Bioingénierie', Strasbourg, France.
Gabriele V; Department of Obstetrics and Gynecology, Strasbourg University Hospital, Strasbourg, France.
Weingertner AS; Department of Obstetrics and Gynecology, Strasbourg University Hospital, Strasbourg, France.
Ruano R; Texas Children's Fetal Center and Baylor College of Medicine, Houston, TX, USA.
Sanz-Cortes M; Texas Children's Fetal Center and Baylor College of Medicine, Houston, TX, USA.
Gaudineau A; Department of Obstetrics and Gynecology, Strasbourg University Hospital, Strasbourg, France.
Langer B; Department of Obstetrics and Gynecology, Strasbourg University Hospital, Strasbourg, France.
Nisand I; Department of Obstetrics and Gynecology, Strasbourg University Hospital, Strasbourg, France.
Akladios CY; Department of Obstetrics and Gynecology, Strasbourg University Hospital, Strasbourg, France.
Favre R; Department of Obstetrics and Gynecology, Strasbourg University Hospital, Strasbourg, France.
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Źródło :
Prenatal diagnosis [Prenat Diagn] 2016 Dec; Vol. 36 (12), pp. 1139-1145. Date of Electronic Publication: 2016 Nov 15.
Typ publikacji :
Journal Article
MeSH Terms :
Brain/*diagnostic imaging
Cerebral Hemorrhage/*diagnostic imaging
Fetal Therapies/*methods
Fetofetal Transfusion/*surgery
Laser Therapy/*methods
Leukomalacia, Periventricular/*diagnostic imaging
Neurodevelopmental Disorders/*physiopathology
Porencephaly/*diagnostic imaging
Adult ; Cerebral Hemorrhage/epidemiology ; Cerebral Ventricles/diagnostic imaging ; Child, Preschool ; Cohort Studies ; Echoencephalography ; Female ; Humans ; Leukomalacia, Periventricular/epidemiology ; Magnetic Resonance Imaging ; Neurodevelopmental Disorders/epidemiology ; Porencephaly/epidemiology ; Pregnancy ; Prospective Studies ; Surveys and Questionnaires ; Twins, Monozygotic ; Young Adult
Czasopismo naukowe
Tytuł :
Porencephaly and Periventricular Encephalitis in a 4-month-old Puppy: Detection of Canine Parvovirus Type 2 and Potential Role in Brain Lesions.
Autorzy :
Marenzoni ML; Department of Veterinary Medicine, University of Perugia, via S. Costanzo n. 4, Perugia, Italy. Electronic address: .
Calò P; Polo Neurologico Veterinario, via Fondo Ausa 48, Dogana, Republic of San Marino and.
Foiani G; Department of Veterinary Medicine, University of Perugia, via S. Costanzo n. 4, Perugia, Italy.
Tossici S; Department of Veterinary Medicine, University of Perugia, via S. Costanzo n. 4, Perugia, Italy.
Passantino G; Department of Veterinary Medicine, University of Bari, Strada Provinciale per Casamassima Km 3, Valenzano, Bari, Italy.
Decaro N; Department of Veterinary Medicine, University of Bari, Strada Provinciale per Casamassima Km 3, Valenzano, Bari, Italy.
Mandara MT; Department of Veterinary Medicine, University of Perugia, via S. Costanzo n. 4, Perugia, Italy.
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Źródło :
Journal of comparative pathology [J Comp Pathol] 2019 May; Vol. 169, pp. 20-24. Date of Electronic Publication: 2019 May 10.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Dog Diseases/*pathology
Dog Diseases/*virology
Encephalitis, Viral/*veterinary
Parvoviridae Infections/*veterinary
Porencephaly/*veterinary
Animals ; Dogs ; Female ; Parvovirus, Canine
Czasopismo naukowe
Tytuł :
Neuroepidemiology of Porencephaly, Schizencephaly, and Hydranencephaly in Miyagi Prefecture, Japan.
Autorzy :
Hino-Fukuyo N; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
Togashi N; Department of Neurology, Miyagi Children's Hospital, Sendai, Japan.
Takahashi R; Neonatal Intensive Care Unit in Perinatal Center, Japanese Red Cross Sendai Hospital, Sendai, Japan.
Saito J; Neonatal Intensive Care Unit, Miyagi Children's Hospital, Sendai, Japan.
Inui T; Department of Pediatric Neurology, Takuto Rehabilitation Center for Children, Sendai, Japan.
Endo W; Department of Pediatric Neurology, Takuto Rehabilitation Center for Children, Sendai, Japan.
Sato R; Department of Pediatric Neurology, Takuto Rehabilitation Center for Children, Sendai, Japan.
Okubo Y; Department of Pediatric Neurology, Takuto Rehabilitation Center for Children, Sendai, Japan.
Saitsu H; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Haginoya K; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan; Department of Pediatric Neurology, Takuto Rehabilitation Center for Children, Sendai, Japan. Electronic address: .
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Źródło :
Pediatric neurology [Pediatr Neurol] 2016 Jan; Vol. 54, pp. 39-42.e1. Date of Electronic Publication: 2015 Aug 28.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Hydranencephaly/*epidemiology
Porencephaly/*epidemiology
Schizencephaly/*epidemiology
Adult ; Brain/pathology ; Female ; Humans ; Hydranencephaly/pathology ; Incidence ; Japan/epidemiology ; Magnetic Resonance Imaging ; Male ; Porencephaly/pathology ; Prevalence ; Schizencephaly/pathology ; Young Adult
Czasopismo naukowe
Tytuł :
Porencephaly in dogs and cats: relationships between magnetic resonance imaging (MRI) features and hippocampal atrophy.
Autorzy :
Hori A; Department of Small Animal Clinical Sciences, School of Veterinary Medicine, Rakuno Gakuen University, 582-1 Bunkyoudai-Midorimachi, Ebetsu, Hokkaido 069-8501, Japan.
Hanazono K
Miyoshi K
Nakade T
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Źródło :
The Journal of veterinary medical science [J Vet Med Sci] 2015 Jul; Vol. 77 (7), pp. 889-92. Date of Electronic Publication: 2015 Mar 16.
Typ publikacji :
Journal Article
MeSH Terms :
Cat Diseases/*diagnosis
Dog Diseases/*diagnosis
Hippocampus/*pathology
Porencephaly/*veterinary
Animals ; Atrophy ; Cat Diseases/pathology ; Cats ; Dog Diseases/pathology ; Dogs ; Female ; Magnetic Resonance Imaging/veterinary ; Male ; Porencephaly/diagnosis ; Porencephaly/pathology
Czasopismo naukowe
Tytuł :
Antenatal diagnosis of intracranial haemorrhage and porencephalic cyst.
Autorzy :
Williams T; Simpson Centre for Reproductive Health, Royal Infirmary of Edinburgh, Edinburgh, UK.
Wilkinson AG; Department of Radiology, Royal Hospital for Sick Children, Edinburgh, UK.
Kandasamy J; Department of Neurosurgery, Royal Hospital for Sick Children, Edinburgh, UK.
Cooper S; Simpson Centre for Reproductive Health, Royal Infirmary of Edinburgh, Edinburgh, UK.
Boardman JP; University of Edinburgh / MRC Centre for Reproductive Health, Edinburgh, UK.
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Źródło :
BMJ case reports [BMJ Case Rep] 2015 Feb 25; Vol. 2015. Date of Electronic Publication: 2015 Feb 25.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Magnetic Resonance Imaging*
Prenatal Diagnosis*
Intracranial Hemorrhages/*complications
Intracranial Hemorrhages/*diagnosis
Porencephaly/*complications
Porencephaly/*diagnosis
Adult ; Brain/pathology ; Brain/surgery ; Cysts ; Female ; Humans ; Infant, Newborn ; Porencephaly/surgery ; Pregnancy
Czasopismo naukowe
Tytuł :
A porencephalic cyst formation in a 6-year-old female with a functioning ventriculoperitoneal shunt: a case-based review.
Autorzy :
Park HJ; Department of Neurosurgery, Seoul National University, College of Medicine, Seoul, Republic of Korea.
Lee SH; Department of Radiology, National Cancer Center, Goyang, Republic of Korea.
Park HJ; Center for Pediatric Cancer, National Cancer Center, Goyang, Republic of Korea.
Shin SH; Neuro-oncology Clinic, National Cancer Center, 323 Ilsan-ro, Ilsandong-gu, Goyang-si, Gyeonggi-do, 10408, Republic of Korea. .
Pokaż więcej
Źródło :
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery [Childs Nerv Syst] 2018 Apr; Vol. 34 (4), pp. 611-616. Date of Electronic Publication: 2018 Jan 29.
Typ publikacji :
Case Reports; Journal Article; Review
MeSH Terms :
Cysts/*complications
Cysts/*surgery
Porencephaly/*complications
Porencephaly/*surgery
Ventriculoperitoneal Shunt/*methods
Cerebrospinal Fluid ; Child ; Female ; Humans
Czasopismo naukowe

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