Results 131 to 140 of about 12,201 (238)

MELAS en el Perú: reporte de caso.

, 2015
El síndrome de MELAS es una rara citopatía mitocondrial de difícil diagnóstico. Reportamos el caso de una niña de 10 años, que ingresó al Instituto Nacional de Ciencias Neurológicas de Lima, Perú, quien presentó episodios bruscos similares a accidentes ...
Escalante-Gavancho, Carlos, Candia-Rivera, Elizabeth, Vattuone-Echevarría, Jorge A., Escalante-Canorio, Jorge, Isidro-Huarcaya, Jaime   +4 more
core   +1 more source

Maria Adele Melas

, 1886
Photograph shows a studio portrait of Maria Adele ...
C. H. Savage (San Antonio, Tex.)
core  

SIDEROBLASTIC ANAEMIA–A HITHERTO UNRCCGNIZED CAUSE OF UNEXPLAINED ANAEMIA

Pakistan Armed Forces Medical Journal, 2018
Objective: To assess the clinicopathological heterogeneity of sideroblastic anemia disorders characterized by the presence of ring sideroblasts in the bone marrow. Study Design: Descriptive study. Place and Duration of Study: Study was conducted
Kamran Nazir Ahmad, Shawana Kamran, Tariq Sarfraz, Khurshid Ali Bangash, Aniqa Bano, Farah Bano   +5 more
doaj  

Barbara Zerr Melas

, 1882
Photograph shows a studio portrait of Barbara Zerr ...
C. H. Savage (San Antonio, Tex.)
core  

MELAS point mutation with unusual clinical presentation

, 1993
Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) is a multisystemic mitochondrial disorder (Pavlakis et al. Advances in Contemporary Neurology.
Silvestri G.
core   +1 more source

Letter to the Editor: Gastrointestinal Pseudo‐Obstruction Is Not an Uncommon Phenotypic Manifestation of POLG1 Variants—Authors' Reply

European Journal of Neurology, Volume 33, Issue 6, June 2026.
Giuliana Capece, Renzo Manara, Leonardo Salviati, Carlo Viscomi, Luca Bello, Elena Pegoraro   +5 more
wiley   +1 more source

beta-Lapachone attenuates mitochondrial dysfunction in MELAS cybrid cells

, 2014
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a mitochondrial disease caused by mutations in the mitochondrial genome.
Park, Woo Jin, Jeong, Moon Hee, Seo, Kang-sik, Kim, Jin Hwan, Kwak, Tae Hwan   +4 more
core   +1 more source

Polemochartus melas

, 2007
Polemochartus melas (GIRAUD, 1863) – 1 ♀ + 3 ♂: KU 22. – A Palaeartic and fairly frequent species. New to the fauna of Korea.Published as part of Papp, J., 2007, Braconidae (Hymenoptera) From Korea Xxii. Subfamily Alysiinae, pp.
Papp, J.
core   +1 more source

Endocrine manifestations and long-term outcomes of patients with mitochondrial diseases

Orphanet Journal of Rare Diseases
Background Endocrine dysfunctions are commonly associated with mitochondrial diseases. This study aimed to investigate clinical characteristics and outcomes of endocrine manifestations in patients with mitochondrial diseases.
Ja Hye Kim, Dohyung Kim, Soojin Hwang, Gu-Hwan Kim, Beom Hee Lee, Han-Wook Yoo, Jin-Ho Choi   +6 more
doaj   +1 more source

MELAS: Clinical features, biochemistry, and molecular genetics

, 1992
We studied 23 patients with clinically defined mitochondrial encephalomyopathy, lactic acidosis, and stroke‐like episodes (MELAS), 25 oligosymptomatic or asymptomatic maternal relatives, and 50 mitochondrial disease control subjects for the presence of a
Angelini C., Martinuzzi A., Bonilla E., Donati M. A., Rowland L. P., DiMauro S., Ciafaloni E., Zammarchi E., Moraes C. T., Servidei S., Silvestri G., Simonetti S., Ricci E., Hirano M., Mosewich R., Shanske S., DeVivo D. C., Schon E. A., Garcia C.   +18 more
core   +1 more source