about
Mitochondrial metabolism in Parkinson's disease impairs quality control autophagy by hampering microtubule-dependent traffic.Neonatal liver failure due to deoxyguanosine kinase deficiencyGenetic basis of Alzheimer's dementia: role of mtDNA mutations.Argininemia and plasma arginine bioavailability - predictive factors of mortality in the severe trauma patients?Antenatal manifestations of mitochondrial disorders.Metabolic effects of hypoxia in colorectal cancer by 13C NMR isotopomer analysis.Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders.Mitochondrial-dependent apoptosis in Huntington's disease human cybrids.Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report.Mitochondrial dysfunction in autism spectrum disorders: a population-based study.The hidden story behind gender differences in familial amyloid polyneuropathy (FAP) ATTRV30M.Pediatric mitochondrial respiratory chain disorders in the Centro region of Portugal.Mitochondrial DNA variants in a portuguese population of patients with Alzheimer's disease.Frontotemporal dementia and mitochondrial DNA transitions.In silico analysis for predicting pathogenicity of five unclassified mitochondrial DNA mutations associated with mitochondrial cytopathies' phenotypes.Value of brain magnetic resonance imaging in mitochondrial respiratory chain disorders.The brain-heart connection in mitochondrial respiratory chain diseases.Mitochondrial DNA 8993T>G mutation in a child with ornithine transcarbamylase deficiency and leigh syndrome: an unexpected association.Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant.mtDNA copy number associated with age of onset in familial amyloid polyneuropathy.Identification of a novel deletion in SURF1 gene: Heterogeneity in Leigh syndrome with COX deficiency.Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene.Genetic Variation of MT-ND Genes in Frontotemporal Lobar Degeneration: Biochemical Phenotype-Genotype Correlation.Long term cortical plasticity in visual retinotopic areas in humans with silent retinal ganglion cell loss.Genotyping CYP2D6 by three different methods: advantages and disadvantages.Citrullinemia stimulation test in the evaluation of the intestinal function.Parkinson's disease and mitochondrial DNA NADH dehydrogenase subunit 1 nucleotides 3337-3340: study in a population from the central region of Portugal (Coimbra).Glutaminemia prognostic significance in critical surgical patients - An analysis of plasma aminogram profile.Nonketotic hyperglycinemia: a cause of encephalopathy in children.Influence of apolipoprotein E genotype on blood redox status of Alzheimer's disease patients.Coenzyme Q₁₀ deficiency in mitochondrial DNA depletion syndromes.High frequency and founder effect of the CYP3A4*20 loss-of-function allele in the Spanish population classifies CYP3A4 as a polymorphic enzymeCharacterization of CYP2D6 genotypes and metabolic profiles in the Portuguese population: pharmacogenetic implicationsResponse to “In silico prediction is insufficient to assess pathogenicity of mtDNA variants”Intestinal dysfunction in the critical trauma patients – An early and frequent eventMitochondrial Respiratory Chain: Biochemical Analysis and Criterion for Deficiency in DiagnosisA study of the electrochemical oxidation of NavelbineCYP2D6 Pharmacogenetics Testing and Post-Cesarean Section Pain Scores-a Preliminary StudyGenomic Ancestry, CYP2D6, CYP2C9, and CYP2C19 Among Latin Americans
P50
Q30525658-19A90035-C18A-44F5-AD04-FF87FA57A573Q35919434-D446E29E-9611-432D-9E9E-7247EDFBAB31Q36471814-D0FFBEC5-F495-47C9-BFF9-65B39085D2CBQ37220937-4BE6820B-9339-48E2-BE53-0C8DED087EFCQ38077672-DA28EC86-D2BE-4226-A7F1-A7750C0F1F6DQ38968639-3D6A06AA-03FA-465B-A282-2FD0CBDAE1B4Q39634938-EFB84A1B-964D-4883-ADB5-EC6E34FAFF96Q39751441-461EECC8-4568-4ADC-B9B7-828B305F5AE4Q43413274-3D2FB4A4-2466-4E28-9989-500B40545CA2Q45288693-5499CE11-479D-4054-A121-FBC3D3FF722DQ45851426-D87F72F7-4191-41BA-A3BE-AD3BEEE60697Q46044027-55D1C3EC-6AE3-41D9-A44D-B2095744186FQ47805998-D7747530-2FE0-414D-A6DC-9DF9EB17495BQ47986294-1D44C064-8929-4DD1-80D6-1B8CF33AB4B6Q48010648-7AB76530-36D4-43DC-99A4-A04506548870Q48305617-8F14603F-16BD-43F3-A560-7D20AC4D4692Q48383509-9005A0F0-3067-4BB0-B206-63A0FB7F1BBFQ48715123-05B051B8-A2B5-407C-BB87-811E390BBD32Q49342881-9ECE7763-8282-458D-99E5-F033452F2A0FQ50091454-BC8C4B2C-3383-418E-A97C-CE13F8123E04Q50195458-46D8D4F8-9282-46A8-8ADE-E7B77ADB6CC9Q50302132-8A41CA3C-7E1A-44EF-8888-EF49D58DDB38Q50590148-7C67DAD7-8392-4E16-9D6B-7A0FC5727450Q50743869-B57B9622-0F98-4F18-94CC-024F1613E14DQ50906654-BD2CAD0E-1680-4530-9226-94121AAC4ED2Q51338428-7F7D2506-1E23-478F-B251-EEEF2044E430Q52806392-6D4C8CCF-1C92-4DA2-87AF-9ACB2B764522Q52821634-A1428FF3-B9BF-42CB-96D1-ACDB095AA459Q53172430-83C4575A-BAD3-4C9F-A421-15E82A2471EDQ53229368-1B2ABB9A-CFED-453A-9A61-6E559CDFBA19Q53771890-E58641F9-938D-4A80-AAF9-7D23B1AC8279Q57083779-20A564EC-E449-4A43-B2D2-714855340F5FQ57585736-AD32EF06-F45C-44D9-931E-C542735882B5Q59848342-7F1FDBE1-7947-482D-B90B-7A6877966D45Q59848406-FC6542D8-8C6F-4D6A-9F96-7DD5F5B98C9BQ59848817-0C640F2A-E976-45B9-9645-91C690A00335Q59849022-DA524C4E-7EC4-4882-AF01-57C60679D20BQ61838025-639DBEA2-D012-45A8-93AE-08612AC86811Q92380175-CDDE22BC-7E74-440A-9716-68CE2BAFCF0A
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Manuela Grazina
@ast
Manuela Grazina
@en
Manuela Grazina
@es
Manuela Grazina
@nl
Manuela Grazina
@sl
type
label
Manuela Grazina
@ast
Manuela Grazina
@en
Manuela Grazina
@es
Manuela Grazina
@nl
Manuela Grazina
@sl
prefLabel
Manuela Grazina
@ast
Manuela Grazina
@en
Manuela Grazina
@es
Manuela Grazina
@nl
Manuela Grazina
@sl
P1053
W-3759-2017
P106
P1153
6507338176
P21
P31
P3829
P496
0000-0002-1173-6481
P569
2000-01-01T00:00:00Z