About: Neurological involvement in hereditary transcobalamin II deficiency

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About: Neurological involvement in hereditary transcobalamin II deficiency Goto Sponge NotDistinct Permalink

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scientific article published on January 1982

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 1982 (ast) наукова стаття, опублікована в січні 1982 (uk) scientific article published on January 1982 (en) مقالة علمية نشرت في يناير 1982 (ar)
publication date	wds:Q37017900-0C0544EA-435D-46F3-B68A-9DE3F8092BDB
publication date	1982-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37017900-05C8C741-63F4-4977-93EB-9A1F7216D939
language of work or name	English
cites work	wds:Q37017900-02E2045E-9EB0-4B06-B8D0-A85111D52A4E wds:Q37017900-0E450629-7297-4F03-9BB6-6490CEC3F5D2 wds:Q37017900-0EFD4338-3057-49FD-8FE6-E39F4F71B210 wds:Q37017900-1AA55244-9DCB-47D5-8A3F-1ED9ED593C20 wds:Q37017900-257AE474-F883-4C9D-9587-E5D2E4AB6199 wds:Q37017900-378BBEAD-97E1-4976-9D6F-0A85F120AF8B wds:Q37017900-4A00169A-00AF-4F8E-A76A-EB7283896EE2 wds:Q37017900-52DF2156-4B0E-44F1-A31C-CB3E1F06C9B6 wds:Q37017900-88C037B7-C296-4657-A849-30CE98125E91 wds:Q37017900-8B8AFCE5-665A-456D-B740-5BB70D307F3C wds:Q37017900-A433E6D5-E995-48E1-9787-99190BA85F52 wds:Q37017900-A483C8A8-3FC6-4315-B48A-BE04A2D0DA6B wds:Q37017900-C974F4AE-5AE3-4CF7-B5C1-C5C072D6C6C2 wds:Q37017900-F04F4651-2710-40EA-8F6E-1042B23AE7CC wds:Q37017900-F30774F5-75E6-42EE-8CA4-F77A0FA204B5 wds:Q37017900-F351776E-AFFB-4BE2-ABAB-19E3C97ED739 wds:Q37017900-FF66DC00-72EA-44DD-BF98-7FDF6790691B
cites work	Dihydrofolate reductase deficiency causing megaloblastic anemia in two families Hereditary transcobalamin II deficiency: clinical findings in a new family Neonatal Megaloblastic Anemia Due to Inherited Transcobalamin II Deficiency in Two Siblings Animal model for subacute combined degeneration Megaloblastic haemopoiesis in patients receiving nitrous oxide Myeloneuropathy after prolonged exposure to nitrous oxide Studies of a patient with megaloblastic anemia and an abnormal transcobalamin II Metabolism of Propionic Acid in Animal Tissues Spinal somatosensory evoked potentials in hereditary spastic paraplegia Inherited Lack of Transcobalamin II in Serum and Megaloblastic Anaemia: a Further Patient Cerebral manifestations of vitamin-B12 deficiency Pathogenesis of subacute combined degeneration: a result of methyl group deficiency Methyl group deficiency in nerve tissue: A hypothesis to explain the lesion of subacute combined degeneration Psychiatric aspects of pernicious anaemia: a prospective controlled investigation. Neurophysiological study of subacute combined degeneration Abnormal propionic-methylmalonic-succinic acid metabolism in vitamin B12 deficiency and its possible relationship to the neurologic syndrome of pernicious anemia The electroencephalogram in pernicious anaemia and subacute combined degeneration of the cord
author name string	wds:Q37017900-31328AFC-26BB-45EE-A86F-47214E9C87CD wds:Q37017900-321E5F26-B734-483F-929D-8260EA37FFAD wds:Q37017900-A42FAA4E-D5D6-4404-A0A2-742CCAE93A51
author name string	Hoffbrand AV Thomas PK Smith IS
rdfs:label	Neurological involvement in hereditary transcobalamin II deficiency (en) Neurological involvement in hereditary transcobalamin II deficiency (nl) Neurological involvement in hereditary transcobalamin II deficiency (ast)
skos:prefLabel	Neurological involvement in hereditary transcobalamin II deficiency (en) Neurological involvement in hereditary transcobalamin II deficiency (nl) Neurological involvement in hereditary transcobalamin II deficiency (ast)
name	Neurological involvement in hereditary transcobalamin II deficiency (en) Neurological involvement in hereditary transcobalamin II deficiency (nl) Neurological involvement in hereditary transcobalamin II deficiency (ast)
title	wds:Q37017900-B8D0B594-DE0F-4A94-B489-EF6480FACC4B
title	Neurological involvement in hereditary transcobalamin II deficiency (en)
page(s)	wds:Q37017900-F37EE4C1-17D7-4A77-8743-F953B968BBFD
page(s)	74-77
instance of	wds:Q37017900-EDF0CF2C-428F-49E7-904D-CA0D90D80F96
instance of	scholarly article
PubMed ID	wds:Q37017900-D4248E13-BDED-402C-A929-095247BF7EEB
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7062075
PubMed ID	7062075
published in	wds:Q37017900-BD4F9067-860B-4FA7-A088-AF8D9ED637BB
published in	Journal of Neurology, Neurosurgery and Psychiatry
issue	wds:Q37017900-6A353352-E652-401C-A94F-55C08352441E
volume	wds:Q37017900-7E7435A9-6224-4DD6-87AE-6C9B7DB58979
issue	1
volume	45
DOI	wds:Q37017900-81DE8BE5-4C1A-4C18-975E-BD51A5B207D9
DOI	http://dx.doi.org/10.1136/JNNP.45.1.74
DOI	10.1136/JNNP.45.1.74
ResearchGate publication ID	wds:Q37017900-0A9B4E07-421E-4F07-9413-41A52AEB4EE8
ResearchGate publication ID	16137120
PMCID	wds:Q37017900-D9E2E3F6-7DFB-49B1-9DD7-16B4FE6EAA0D
PMCID	491269
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37017900
is cites work of	Methylenetetrahydrofolate reductase and transcobalamin genetic polymorphisms in human spontaneous abortion: biological and clinical implications Folate and homocysteine metabolism in neural plasticity and neurodegenerative disorders Transcobalamin II deficiency: case report and review of the literature. Update on transcobalamin deficiency: clinical presentation, treatment and outcome Long-term neurologic consequences of nutritional vitamin B12 deficiency in infants Genetic patterns of transcobalamin II and the relationships with congenital defects Expression of transcobalamin II mRNA in human tissues and cultured fibroblasts from normal and transcobalamin II-deficient patients

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