Autor: "Kentab AY" - OpacWWW

Skocz do pozycji: 1.

Tytuł:: Auto-immune anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis: three case reports.
Autorzy:: Bashiri FA; a Division of Pediatric Neurology.
Al-Rasheed AA; b Pediatric Rheumatology, Department of Pediatrics.
Hassan SM; a Division of Pediatric Neurology.
Hamad MHA; a Division of Pediatric Neurology.
El Khashab HY; a Division of Pediatric Neurology.
Kentab AY; a Division of Pediatric Neurology.
AlBadr FB; c Division of Neuroradiology, Department of Radiology, College of Medicine and King Khalid University Hospital , King Saud University , Riyadh , Saudi Arabia.
Salih MA; a Division of Pediatric Neurology.; Pokaż więcej
Źródło:: Paediatrics and international child health [Paediatr Int Child Health] 2017 Aug; Vol. 37 (3), pp. 222-226. Date of Electronic Publication: 2016 Jun 22.
Typ publikacji:: Case Reports; Journal Article
MeSH Terms:: Anti-N-Methyl-D-Aspartate Receptor Encephalitis/*diagnosis
Anti-N-Methyl-D-Aspartate Receptor Encephalitis/*pathology
Autoantibodies/*blood
Brain/*diagnostic imaging
Receptors, N-Methyl-D-Aspartate/*immunology
Adrenal Cortex Hormones/therapeutic use ; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/drug therapy ; Child ; Child, Preschool ; Diagnosis, Differential ; Female ; Humans ; Immunoglobulins, Intravenous/therapeutic use ; Immunologic Factors/therapeutic use ; Infant ; Magnetic Resonance Imaging ; Rituximab/therapeutic use ; Treatment Outcome

Czasopismo naukowe

Skocz do pozycji: 2.

Tytuł:: Ophthalmologic observations in a patient with partial mosaic trisomy 8.
Autorzy:: Abu-Amero KK; Department of Ophthalmology and.
Kondkar AA
Salih MA
Al-Husain M
Al Shammari M
Zeidan G
Oystreck DT
Hellani AM
Kentab AY
Bosley TM; Pokaż więcej
Źródło:: Ophthalmic genetics [Ophthalmic Genet] 2013 Dec; Vol. 34 (4), pp. 249-53. Date of Electronic Publication: 2013 Feb 13.
Typ publikacji:: Case Reports; Journal Article
MeSH Terms:: Mosaicism*
Agenesis of Corpus Callosum/*diagnosis
Esotropia/*diagnosis
Trisomy/*diagnosis
Agenesis of Corpus Callosum/genetics ; Chromosomes, Human, Pair 8/genetics ; Comparative Genomic Hybridization ; Esotropia/genetics ; Female ; Genotype ; Humans ; Infant ; Karyotyping ; Magnetic Resonance Imaging ; Pedigree ; Phenotype ; Trisomy/genetics
SCR Disease Name:: Chromosome 8, partial trisomy

Czasopismo naukowe

Skocz do pozycji: 3.

Tytuł:: New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations.
Autorzy:: Salih MA; Division of Pediatric Neurology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Mundwiller E
Khan AO
AlDrees A
Elmalik SA
Hassan HH
Al-Owain M
Alkhalidi HM
Katona I
Kabiraj MM
Chrast R
Kentab AY
Alzaidan H
Rodenburg RJ
Bosley TM
Weis J
Koenig M
Stevanin G
Azzedine H; Pokaż więcej
Źródło:: PloS one [PLoS One] 2013 Oct 09; Vol. 8 (10), pp. e76831. Date of Electronic Publication: 2013 Oct 09 (Print Publication: 2013).
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Mutation*
Phenotype*
Group VI Phospholipases A2/*genetics
Adolescent ; Adult ; Arabs ; Child ; Child, Preschool ; Consanguinity ; Electroencephalography ; Evoked Potentials, Visual/genetics ; Female ; Follow-Up Studies ; Genotype ; Humans ; Infant ; Male ; Muscles/pathology ; Muscles/physiopathology ; Neural Conduction/genetics ; Neuroaxonal Dystrophies/ethnology ; Neuroaxonal Dystrophies/genetics ; Neuroaxonal Dystrophies/pathology ; Neuroaxonal Dystrophies/physiopathology ; Neuroimaging ; Pedigree ; Young Adult
SCR Disease Name:: Karak Syndrome

Czasopismo naukowe

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