Zobrazeno 1 - 10
of 416
pro vyhledávání: '"G N, Thompson"'
Autor:
Joy Arruda
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 7, Iss 1, Pp 82-83
Externí odkaz:
https://doaj.org/article/a21013befb0f4e64b0ba3ba1ea26bb2b
Autor:
Arruda, Joy
Publikováno v:
Arquivos de Neuro-Psiquiatria, Volume: 7, Issue: 1, Pages: 82-83, Published: MAR 1949
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::3c769ab2f2f6274b2eb8bedc973472ed
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1949000100016&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1949000100016&lng=en&tlng=en
Autor:
KARS FERTELLİ, Tülay1 afertelli@gmail.com
Publikováno v:
Journal of Inonu University Health Services Vocational School / Inönü Üniversitesi Sağlık Hizmetleri Meslek Yüksekokulu Dergisi. eki2024, Vol. 12 Issue 3, p946-959. 14p.
Autor:
Charles A. Stanley, Andrew A. M. Morris, Marie-France Robert, Patti Quant, Lyudmila Ashmarina, James V. Leonard, Dmitriy A. Vinarov, Betty Y.L. Hsu, Youssef Boukaftane, Henry M. Miziorko, G. N. Thompson, Grant A. Mitchell, Luigi Bouchard, Shupei Wang, Avihu Boneh
Publikováno v:
Scopus-Elsevier
Hereditary deficiency of mitochondrial HMG-CoA synthase (mHS, OMIM 600234) is a poorly defined, treatable, probably underdiagnosed condition that can cause episodes of severe hypoketotic hypoglycemia. We present clinical follow-up and molecular analy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7005490af0872b211ccc2bb586a759bf
https://doi.org/10.1203/00006450-200103000-00005
https://doi.org/10.1203/00006450-200103000-00005
Publikováno v:
Journal of Inherited Metabolic Disease. 17:74-80
The effect of fasting on plasma concentrations of fatty acids has been determined in four children with medium-chain acyl-CoA dehydrogenase (MCAD) deficiency. In addition, the in vivo rate of octanoate oxidation was measured, using [1-13C]octanoate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b3a56ab2a3c7cae228a5c11fb09fb22
https://doi.org/10.1007/bf00735398
https://doi.org/10.1007/bf00735398
Publikováno v:
Aging Psychology. Aug2024, Vol. 10 Issue 2, p221-242. 22p.
Publikováno v:
Journal of Inherited Metabolic Disease. 16:942-949
Succinic semialdehyde dehydrogenase (SSAD) is an enzyme involved in the turnover of the neurotransmitter 4-aminobutyrate (GABA). Deficiency of SSAD results in developmental delay, ataxia, seizures and 4-hydroxybutyric aciduria. We have developed a si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a382767b7b4f033479d41c550230831f
https://doi.org/10.1007/bf00711509
https://doi.org/10.1007/bf00711509
Autor:
G N, THOMPSON
Publikováno v:
The American journal of psychiatry. 102
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::262889218c935ea2fb246e02440a43fd
https://pubmed.ncbi.nlm.nih.gov/21007690
https://pubmed.ncbi.nlm.nih.gov/21007690
Autor:
W R, ROSANOFF, G N, THOMPSON
Publikováno v:
Annals of western medicine and surgery. 1(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0dc4ecff8ed6cd7e43e6585b72327772
https://pubmed.ncbi.nlm.nih.gov/20272387
https://pubmed.ncbi.nlm.nih.gov/20272387
Autor:
G N, THOMPSON
Publikováno v:
Bulletin of the Los Angeles Neurological Society. 12(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2f1095863f98e3666b8994c42d36d401
https://pubmed.ncbi.nlm.nih.gov/20254477
https://pubmed.ncbi.nlm.nih.gov/20254477