Evidence of insulin resistance and other metabolic alterations in boys with Duchenne or Becker muscular dystrophy
M Rodríguez-Cruz, R Sanchez… - International Journal …, 2015 - Wiley Online Library
Aim. Our aim was (1) to determine the frequency of insulin resistance (IR) in patients with
Duchenne/Becker muscular dystrophy (DMD/BMD),(2) to identify deleted exons of DMD …
Duchenne/Becker muscular dystrophy (DMD/BMD),(2) to identify deleted exons of DMD …
Evidence of muscle loss delay and improvement of hyperinsulinemia and insulin resistance in Duchenne muscular dystrophy supplemented with omega-3 fatty acids …
M Rodríguez-Cruz, S Atilano-Miguel, L Barbosa-Cortés… - Clinical nutrition, 2019 - Elsevier
Summary Background & aims Duchenne Muscular Dystrophy (DMD) is the most prevalent
dystrophy of childhood and is characterized by generalized motor delays due to progressive …
dystrophy of childhood and is characterized by generalized motor delays due to progressive …
[HTML][HTML] Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach
AA Freund, RH Scola, RC Arndt… - Arquivos de neuro …, 2007 - SciELO Brasil
Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are caused by
mutations in the dystrophin gene. We studied 106 patients with a diagnosis of probable …
mutations in the dystrophin gene. We studied 106 patients with a diagnosis of probable …
Predominance of dystrophinopathy genotypes in mexican male patients presenting as muscular dystrophy with a normal multiplex polymerase chain reaction DMD …
MA Alcántara-Ortigoza, ME Reyna-Fabián… - Genes, 2019 - mdpi.com
The complete mutational spectrum of dystrophinopathies and limb-girdle muscular
dystrophy (LGMD) remains unknown in Mexican population. Seventy-two unrelated Mexican …
dystrophy (LGMD) remains unknown in Mexican population. Seventy-two unrelated Mexican …
Clinical, immunohistochemical, Western blot, and genetic analysis in dystrophinopathy
SJ Na, WJ Kim, SM Kim, KO Lee, B Yoon… - Journal of Clinical …, 2013 - Elsevier
Dystrophin-deficient muscular dystrophies (dystrophinopathies) are the most common form
of muscular dystrophy, with variable clinical phenotypes ranging from the severe Duchenne …
of muscular dystrophy, with variable clinical phenotypes ranging from the severe Duchenne …
[PDF][PDF] Distrofias musculares en México: un enfoque clínico, bioquímico y molecular
RMC Vázquez, LBL Hernández… - Revista de …, 2010 - redalyc.org
Las distrofias musculares son un conjunto de enfermedades que se distinguen por
debilidad progresiva y desgaste muscular que generalmente provocan discapacidad. En …
debilidad progresiva y desgaste muscular que generalmente provocan discapacidad. En …
Duchenne muscular dystrophy in a developing country: challenges in management and genetic counseling
LB López-Hernández, B Gomez-Diaz… - Genetic …, 2014 - search.proquest.com
Abstract Multidisciplinary management of Duchenne Muscular Dystrophy (DMD) has
achieved outstanding results in developed nations. We aimed to describe the status of …
achieved outstanding results in developed nations. We aimed to describe the status of …
Comparative analysis of PCR‐deletion detection and immunohistochemistry in Brazilian Duchenne and Becker muscular dystrophy patients
LC Werneck, RH Scola, GHB Maegawa… - American journal of …, 2001 - Wiley Online Library
We studied 48 patients with dystrophinopathies (29 Duchenne muscular dystrophy (DMD),
13 Becker muscular dystrophy (BMD), four possible carriers, one female with DMD, and one …
13 Becker muscular dystrophy (BMD), four possible carriers, one female with DMD, and one …
Log-PCR: a new tool for immediate and cost-effective diagnosis of up to 85% of dystrophin gene mutations
Abstract Background: Duchenne (DMD) and Becker (BMD) muscular dystrophies are
caused by mutations in the dystrophin gene. Despite the progress in the technologies of …
caused by mutations in the dystrophin gene. Despite the progress in the technologies of …
RET oncogene mutations in medullary thyroid carcinoma in Mexican families
B González, M Salcedo, ME Medrano, A Mantilla… - Archives of medical …, 2003 - Elsevier
BACKGROUND: Different RET oncogene mutations have been found to be associated with
inherited medullary thyroid carcinoma (MTC) in the context of three different syndromes …
inherited medullary thyroid carcinoma (MTC) in the context of three different syndromes …