Zobrazeno 1 - 10 of 115 pro vyhledávání: '"George A. Jervis"'
1
An unusual type of infantile lipofuscinosis
Autor: George A. Jervis, Sheila Donahue
Publikováno v: Acta Neuropathologica. 31:109-116
The case of a child is described who at the age of 2 years showed the first evidence of a developing neurological disease. Within a couple of years, profound mental retardation and severe motor deficit with spastic tetraplegia became established. No
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e59b97043193c919a83a0246ec1c9ff8
https://doi.org/10.1007/bf00688145
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2
Alzheimer neurofibrillary tangles in diseases other than senile and presenile dementia
Autor: Henryk M. Wisniewski, Krystyna E. Wisniewski, Roger C. Moretz, George A. Jervis
Publikováno v: Annals of Neurology. 5:288-294
A brief description is given of neurofibrillary changes of the paired helical filament type in a variety of chronic neurological diseases. These include subacute sclerosing panencephalitis, lead encephalopathy, tuberous sclerosis, Down syndrome, Hall
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a94cf23f4e858631f2f8264992136897
https://doi.org/10.1002/ana.410050311
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3
DEVELOPMENTAL RETARDATION ASSOCIATED WITH AN ABNORMALITY IN TYROSINE METABOLISM
Autor: John H. Menkes, George A. Jervis
Publikováno v: Pediatrics. 28:399-409
An infant with seizures, spasticity, and failure in weight gain was shown to excrete p-hydroxyphenylpyruvic acid, p-hydroxyphenyllactic acid, and p-hydroxyphenylacetic acid, indicating the likelihood of an impairment in the oxidation of p-hydroxyphen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e5886cdad43b8262c2b421751ac363f7
https://doi.org/10.1542/peds.28.3.399
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7
The Genetics of Phenylpyruvic Oligophrenia
Autor: George A. Jervis
Publikováno v: Journal of Mental Science. 85:719-762
Although considerable attention has been devoted during the past years to the problems of the influence of heredity on mental deficiency, no final conclusions have yet been reached. It appears well established at the present time, first, that in a la
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::127ec9907ff33255d1dfe75170cab688
https://doi.org/10.1192/bjp.85.357.719
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8
Detection of heterozygotes for phenylketonuria
Autor: George A. Jervis
Publikováno v: Clinica Chimica Acta. 5:471-476
A method is described which can be used to detect the heterozygote (carrier) for phenylketonuria. It is based on the determination of blood tyrosine at various intervals following the ingestion of a large dose (2 mmoles/kg) of l -phenylalanine. The t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9196bb9866ecceb237fbf4f38c0ba24a
https://doi.org/10.1016/0009-8981(60)90054-1
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