Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family

scientific article published on 01 March 2001

Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1212/WNL.56.6.802
P698PubMed publication ID11274324

P50authorFilippo Maria SantorelliQ60541206
P2093author name stringG Casari
D Fortini
F Pierelli
V Bonifati
R Carrozzo
G Meco
C Casali
N Vanacore
G D'Amati
G Fabbrini
N Locuratolo
M Damiano
A Patrignani
A Pierallini
G A Amabile
P433issue6
P921main subjectParkinson's diseaseQ11085
parkinsonian syndromeQ1531991
mitochondrial myopathyQ6881881
P1104number of pages4
P304page(s)802-805
P577publication date2001-03-01
P1433published inNeurologyQ1161692
P1476titleMitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family
P478volume56

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Q28188428Digenic progressive external ophthalmoplegia in a sporadic patient: recessive mutations in POLG and C10orf2/Twinkle
Q42132131Do somatic mitochondrial DNA mutations contribute to Parkinson's disease?
Q33548162Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease
Q89467884Mitochondrial DNA m.13514G>A heteroplasmy is associated with depressive symptoms in the elderly
Q28710285Mitochondrial DNA sequence variation and neurodegeneration
Q30444758Mitochondrial dysfunction and oxidative stress in Parkinson's disease.
Q64088274Muscle Biopsy: A Boon for Diagnosis of Mitochondrial Parkinsonism in Developing Countries
Q53612457Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.
Q35166737Progressive external ophthalmoplegia characterized by multiple deletions of mitochondrial DNA: unraveling the pathogenesis of human mitochondrial DNA instability and the initiation of a genetic classification
Q34174847Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia

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