Results 161 to 170 of about 9,186 (248)

Mitochondrial cardiomyopathy with skeletal muscle myopathy caused by m.3260A > G mutation in MT-TL1 gene: a case report. [PDF]

J Med Case Rep
Kadiša A, Vereskuns R, Tarasovs M, Mičule I, Inashkina I.   +4 more
europepmc   +1 more source

Mitochondrial cardiomyopathies: navigating through different clinical and management pictures between adult and paediatric forms. [PDF]

Front Cardiovasc Med
Adorisio R, Cantarutti N, Siri B, Bellettini E, Ingrasciotta G, Mencarelli E, Graziani F, Lillo R, Di Marzio S, Di Mambro C, Drago F, Amodeo A, Martinelli D.   +12 more
europepmc   +1 more source

Third Nerve Palsy: A Case of Bilateral Eyelid Ptosis, Normal Pupils, and Vertical Diplopia With Multiple Intracranial Lesions. [PDF]

Cureus
Dragomir RM, Carranza-Rentería O, Swerdloff MA, Kay M.   +3 more
europepmc   +1 more source

Diagnostic Value of Muscle Biopsy for the Evaluation of Adult Myopathy in Daily Clinical Practice. [PDF]

Diagnostics (Basel)
Kleinveld VEA, Wanschitz J, Hotter A, Mayr JA, Höftberger R, Löscher WN, Horlings CGC.   +6 more
europepmc   +1 more source

Pediatric Hepatology: A three-year experience with pediatric liver transplantation with cyclosporine and steroids [PDF]

, 1986
Gartner, JC, Iwatsuki, S, Malatack, JJ, Shaw, BW, Starzl, TE, Urbach, AH, Zitelli, BH   +6 more
core  

Mitochondrial DNA Replication and Disease: A Historical Perspective on Molecular Insights and Therapeutic Advances. [PDF]

Int J Mol Sci
Somai S, Aloh CH, King DE, Copeland WC.
europepmc   +1 more source

Anti-GQ1b Antibody Syndrome: A Clinician-Oriented Perspective on Diagnostics, Therapy, and Atypical Phenotypes-With an Illustrative 16-Case Institutional Series. [PDF]

J Clin Med
Bannai T, Yamada M, Seki T, Shiio Y, Yamasoba T.   +4 more
europepmc   +1 more source

Severe clinical manifestation of mitochondrial disease due to the m.3243A>T variant: a case report of early-onset, multi-organ involvement and premature death. [PDF]

J Rare Dis (Berlin)
Gillespie H, Ng YS, Wood KM, Hopton S, Alston CL, Blakely EL, Thompson N, Taylor RW, Browning AC, McFarland R, Sayer JA.   +10 more
europepmc   +1 more source

mtDNA deletion m.8753_16566 with < 10 % heteroplasmy in muscle and isolated complex-V dysfunction misinterpreted as chronic fatigue syndrome over 21-years. [PDF]

Clinics (Sao Paulo)
Finsterer J, Fiorini AC, Scorza FA, Scorza CA.   +3 more
europepmc   +1 more source