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Wyszukujesz frazę ""Scarlato, G."" wg kryterium: Autor


Tytuł :
Malingering and retrograde amnesia: the historic case of the Collegno amnesic.
Autorzy :
Zago S; Dipartimento di Scienze Neurologiche e degli Organi di Senso, IRCCS Ospedale Maggiore-Policlinico, Università di Milano, Italy. />Sartori G
Scarlato G
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Źródło :
Cortex; a journal devoted to the study of the nervous system and behavior [Cortex] 2004 Jun; Vol. 40 (3), pp. 519-32.
Typ publikacji :
Biography; Case Reports; Historical Article; Journal Article; Portrait
MeSH Terms :
Famous Persons*
Amnesia, Retrograde/*history
Malingering/*history
Amnesia, Retrograde/diagnosis ; History, 20th Century ; Humans ; Interview, Psychological ; Italy ; Male ; Malingering/diagnosis ; Neuropsychological Tests/history
Personal Name as Subject :
Coppola A; Bruneri M
Czasopismo naukowe
Tytuł :
Induction of IL-10 in rat peritoneal macrophages and dendritic cells by glatiramer acetate.
Autorzy :
Jung S; Klinische Forschungsgruppe für Multiple Sklerose an der Neurologischen Klinik, Julius-Maximilians-Universität Würzburg, Germany.
Siglienti I
Grauer O
Magnus T
Scarlato G
Toyka K
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Źródło :
Journal of neuroimmunology [J Neuroimmunol] 2004 Mar; Vol. 148 (1-2), pp. 63-73.
Typ publikacji :
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Antigens, CD*
Antigens, Neoplasm*
Antigens, Surface*
Avian Proteins*
Blood Proteins*
Dendritic Cells/*drug effects
Interleukin-10/*metabolism
Macrophages, Peritoneal/*drug effects
Peptides/*pharmacology
Animals ; Antigens, Differentiation/metabolism ; Basigin ; Cells, Cultured ; Dendritic Cells/metabolism ; Dose-Response Relationship, Drug ; Drug Interactions ; Enzyme-Linked Immunosorbent Assay/methods ; Flow Cytometry/methods ; Glatiramer Acetate ; High Mobility Group Proteins/pharmacology ; Immunosuppressive Agents/pharmacology ; Lipopolysaccharides/pharmacology ; Macrophages, Peritoneal/metabolism ; Mast Cells/drug effects ; Membrane Glycoproteins/metabolism ; Myelin Basic Protein/metabolism ; Rats ; Rats, Inbred Lew ; Tumor Necrosis Factor-alpha/metabolism
Czasopismo naukowe
Tytuł :
High mutational burden in the mtDNA control region from aged muscles: a single-fiber study.
Autorzy :
Del Bo R; Centro Dino Ferrari, Centro di Eccellenza per le Malattie Neurodegenerative, Dipartimento di Scienze Neurologiche, Università degli Studi di Milano, I.R.C.C.S. Ospedale Maggiore Policlinico, Via F. Sforza, 35, 20122 Milan, Italy. />Crimi M
Sciacco M
Malferrari G
Bordoni A
Napoli L
Prelle A
Biunno I
Moggio M
Bresolin N
Scarlato G
Pietro Comi G
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Źródło :
Neurobiology of aging [Neurobiol Aging] 2003 Oct; Vol. 24 (6), pp. 829-38.
Typ publikacji :
Journal Article
MeSH Terms :
Aged/*physiology
DNA, Mitochondrial/*genetics
Electron Transport Complex IV/*genetics
Muscle Fibers, Skeletal/*physiology
Muscle, Skeletal/*physiology
Aged, 80 and over ; Biopsy ; DNA Mutational Analysis ; DNA, Mitochondrial/metabolism ; Humans ; Muscle Fibers, Skeletal/enzymology ; Muscle Fibers, Skeletal/pathology ; Muscle, Skeletal/enzymology ; Muscle, Skeletal/pathology ; Point Mutation ; Reference Values
Czasopismo naukowe
Tytuł :
A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome.
Autorzy :
Crimi M; Dino Ferrari Center, Department of Neurological Sciences, University of Milan, I.R.C.C.S. Ospedale Maggiore Policlinico, Italy. />Galbiati S
Moroni I
Bordoni A
Perini MP
Lamantea E
Sciacco M
Zeviani M
Biunno I
Moggio M
Scarlato G
Comi GP
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Źródło :
Neurology [Neurology] 2003 Jun 10; Vol. 60 (11), pp. 1857-61.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Mutation, Missense*
Electron Transport Complex I/*genetics
Leigh Disease/*genetics
MELAS Syndrome/*genetics
Mitochondrial Proteins/*genetics
Adolescent ; Amino Acid Sequence ; Base Sequence ; Brain/pathology ; Genetic Predisposition to Disease ; Humans ; Leigh Disease/diagnosis ; MELAS Syndrome/diagnosis ; Magnetic Resonance Imaging ; Male ; Molecular Sequence Data ; Sequence Alignment
Czasopismo naukowe
Tytuł :
The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects.
Autorzy :
Del Bo R; Dipartimento di Scienze Neurologiche, Padiglione Ponti, I. R. C. S. S. Ospedale Maggiore Policlinico, Via F. Sforza, 35, 20122 Milan, Italy. />Comi GP
Giorda R
Crimi M
Locatelli F
Martinelli-Boneschi F
Pozzoli U
Castelli E
Bresolin N
Scarlato G
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Źródło :
Journal of neurology [J Neurol] 2003 Jun; Vol. 250 (6), pp. 688-92.
Typ publikacji :
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Polymorphism, Genetic*
Cognition Disorders/*genetics
Down Syndrome/*genetics
Prions/*genetics
Adolescent ; Adult ; Age Factors ; Alleles ; Amino Acid Substitution ; Apolipoprotein E4 ; Apolipoproteins E/classification ; Apolipoproteins E/metabolism ; Child ; Child, Preschool ; Codon ; Cognition Disorders/etiology ; Down Syndrome/physiopathology ; Female ; Follow-Up Studies ; Gene Frequency ; Genotype ; Humans ; Intelligence Tests ; Male ; Methionine/genetics ; Mutation ; Valine/genetics
Czasopismo naukowe
Tytuł :
Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency.
Autorzy :
Prelle A; Centro Dino Ferrari, Department of Neurological Sciences, University of Milan, Ospedale Maggiore-Policlinico IRCCS, Via F. Sforza 35, 20122, Milan, Italy. />Sciacco M
Tancredi L
Fagiolari G
Comi GP
Ciscato P
Serafini M
Fortunato F
Zecca C
Gallanti A
Chiveri L
Bresolin N
Scarlato G
Moggio M
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Źródło :
Acta neuropathologica [Acta Neuropathol] 2003 Jun; Vol. 105 (6), pp. 537-42. Date of Electronic Publication: 2003 Mar 04.
Typ publikacji :
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Membrane Proteins*
Muscle Proteins/*deficiency
Muscle Proteins/*metabolism
Muscular Dystrophies/*metabolism
Adolescent ; Adult ; Blotting, Western/methods ; Child ; Dysferlin ; Dystrophin/metabolism ; Evaluation Studies as Topic ; Female ; Humans ; Immunohistochemistry/methods ; Male ; Middle Aged ; Muscle Proteins/genetics ; Muscle, Skeletal/pathology ; Muscular Dystrophies/classification ; Muscular Dystrophies/diagnosis ; Muscular Dystrophies/genetics ; fas Receptor/metabolism
Czasopismo naukowe
Tytuł :
Severe chronic sensory-motor polyneuropathy: coexistence of 3 unrelated etiologies in a type 1 diabetic patient. A case report and review of the literature.
Autorzy :
Micco A; Department of Neurological Sciences, University of Milan, IRCCS Ospedale Maggiore Policlinico, Milan, Italy. />Nobile-Orazio E
Baron P
Conti G
Napoli L
Serafini M
Scarlato G
Scarpini E
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Źródło :
Journal of the peripheral nervous system : JPNS [J Peripher Nerv Syst] 2003 Mar; Vol. 8 (1), pp. 23-8.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms :
Diabetes Mellitus, Type 1/*complications
Diabetic Neuropathies/*etiology
Polyneuropathies/*etiology
Chronic Disease ; Diabetes Mellitus, Type 1/pathology ; Diabetic Neuropathies/pathology ; Humans ; Male ; Middle Aged ; Polyneuropathies/pathology
Czasopismo naukowe

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