Source: Acta neurologica Scandinavica [Acta Neurol Scand] 2019 Jan; Vol. 139 (1), pp. 86-87. Date of Electronic Publication: 2018 Oct 22.Publisher: Wiley-Blackwell Country of Publication: Denmark NLM ID: 0370336 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

MELAS syndrome in a patient with a point mutation in MTTS1.

Authors : Lindberg, Christopher; Moslemi, Ali-Reza; Oldfors, Anders, 1951

Subjects: Cell and Molecular Biology; Cell- och molekylärbiologi; Medical Genetics and Genomics

Source: Acta neurologica Scandinavica. 117(2):128-32

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Absence of maternal A3243G mtDNA mutation and reversible hyperglycemia in a patient with MELAS syndrome: Spontaneous mtDNA mutation in MELAS syndrome

Authors : C.-W. Liou; C.-C. Huang; J.-L. Tsai

Subjects: Adult; Male; Vasculitis

Source: Acta Neurologica Scandinavica. 101:65-69

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MELAS: a neuropsychological and radiological follow-up study. Mitochondrial encephalomyopathy, lactic acidosis and stroke.

Authors : Sartor H; Department of Psychiatry, University of Regensburg, Germany. ; Loose R

Subjects: MELAS Syndrome/MELAS Syndrome/MELAS Syndrome/*diagnostic imaging ; MELAS Syndrome/MELAS Syndrome/MELAS Syndrome/*psychology; Adult

Source: Acta neurologica Scandinavica [Acta Neurol Scand] 2002 Nov; Vol. 106 (5), pp. 309-13.Publisher: Wiley-Blackwell Country of Publication: Denmark NLM ID: 0370336 Publication Model: Print Cited Medium: Print ISSN: 0001-6314 (Print)

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Absence of maternal A3243G mtDNA mutation and reversible hyperglycemia in a patient with MELAS syndrome.

Authors : Liou CW; Department of Neurology, Chang Gung Memorial Hospital, Kaohsiung, Hsien, Taiwan.; Huang CC

Subjects: DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics ; Diabetes Mellitus/Diabetes Mellitus/Diabetes Mellitus/*genetics ; Hyperglycemia/Hyperglycemia/Hyperglycemia/*genetics

Source: Acta neurologica Scandinavica [Acta Neurol Scand] 2000 Jan; Vol. 101 (1), pp. 65-9.Publisher: Wiley-Blackwell Country of Publication: Denmark NLM ID: 0370336 Publication Model: Print Cited Medium: Print ISSN: 0001-6314 (Print)

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MELAS: Monitoring treatment with magnetic resonance spectroscopy.

Authors : Hovsepian, Dominic A.; Galati, Alexandra; Chong, Robert A.

Subjects: NUCLEAR magnetic resonance spectroscopy; ARGININE; LACTIC acidosis

Source: Acta Neurologica Scandinavica; Jan2019, Vol. 139 Issue 1, p82-85, 4p

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Phenøtypes and mitochondrial DNA substitutions in families with A3243G mutation: A3243G mutation and clinical phenotypes

Authors : Itsuro Higuchi; S. Morovvati; Y. Sato

Subjects: Adult; Family Health; Male

Source: Acta Neurologica Scandinavica. 106:104-108

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Outcome of men and women after atrial fibrillation and stroke.

Authors : Jönsson, A.‐C.; Ek, J.; Kremer, C.

Subjects: ATRIAL fibrillation; ATRIAL arrhythmias; CEREBROVASCULAR disease

Source: Acta Neurologica Scandinavica; Aug2015, Vol. 132 Issue 2, p125-131, 7p

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Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.

Authors : Liu CS; Vascular and Genomic Research Center, Changhua Christian Hospital, Changhua, Taiwan.; Cheng WL

Subjects: DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics ; Leukocytes/Leukocytes/Leukocytes/*physiology ; MELAS Syndrome/MELAS Syndrome/MELAS Syndrome/*genetics

Source: Acta neurologica Scandinavica [Acta Neurol Scand] 2006 May; Vol. 113 (5), pp. 334-41.Publisher: Wiley-Blackwell Country of Publication: Denmark NLM ID: 0370336 Publication Model: Print Cited Medium: Print ISSN: 0001-6314 (Print)

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نتائج البحث

فلترة النتائج

MELAS: Monitoring treatment with magnetic resonance spectroscopy

Patients with MELAS not only require treatment of stroke-like episodes but a comprehensive individual and family management.

MELAS syndrome in a patient with a point mutation in MTTS1.

Absence of maternal A3243G mtDNA mutation and reversible hyperglycemia in a patient with MELAS syndrome: Spontaneous mtDNA mutation in MELAS syndrome

MELAS: a neuropsychological and radiological follow-up study. Mitochondrial encephalomyopathy, lactic acidosis and stroke.

Absence of maternal A3243G mtDNA mutation and reversible hyperglycemia in a patient with MELAS syndrome.

MELAS: Monitoring treatment with magnetic resonance spectroscopy.

Phenøtypes and mitochondrial DNA substitutions in families with A3243G mutation: A3243G mutation and clinical phenotypes

Outcome of men and women after atrial fibrillation and stroke.

Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.

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