نتایج جستجو برای: muscular disease

تعداد نتایج: 1522672  

Journal: :Human molecular genetics 2005
Kimberly A Huebsch Elena Kudryashova Christine M Wooley Roger B Sher Kevin L Seburn Melissa J Spencer Gregory A Cox

Human tibial muscular dystrophy and limb-girdle muscular dystrophy 2J are caused by mutations in the giant sarcomeric protein titin (TTN) adjacent to a binding site for the muscle-specific protease calpain 3 (CAPN3). Muscular dystrophy with myositis (mdm) is a recessive mouse mutation with severe and progressive muscular degeneration caused by a deletion in the N2A domain of titin (TTN-N2ADelta...

2014
Karli Montague Bilal Malik Anna L. Gray Albert R. La Spada Michael G. Hanna Gyorgy Szabadkai Linda Greensmith

Spinal and bulbar muscular atrophy is an X-linked degenerative motor neuron disease caused by an abnormal expansion in the polyglutamine encoding CAG repeat of the androgen receptor gene. There is evidence implicating endoplasmic reticulum stress in the development and progression of neurodegenerative disease, including polyglutamine disorders such as Huntington's disease and in motor neuron di...

2016
Davy Vanhoutte Tobias G Schips Jennifer Q Kwong Jennifer Davis Andoria Tjondrokoesoemo Matthew J Brody Michelle A Sargent Onur Kanisicak Hong Yi Quan Q Gao Joseph E Rabinowitz Talila Volk Elizabeth M McNally Jeffery D Molkentin

Skeletal muscle is highly sensitive to mutations in genes that participate in membrane stability and cellular attachment, which often leads to muscular dystrophy. Here we show that Thrombospondin-4 (Thbs4) regulates skeletal muscle integrity and its susceptibility to muscular dystrophy through organization of membrane attachment complexes. Loss of the Thbs4 gene causes spontaneous dystrophic ch...

Journal: :Archives of disease in childhood 1973
J H Pearn J Wilson

Pearn, J. H., and Wilson, J. (1973). Archives of Disease in Childhood, 48, 768. Chronic generalized spinal muscular atrophy of infancy and childhood: arrested Werdnig-Hoffmann disease. Recent studies have shown that the acute fatal form of infantile spinal muscular atrophy (acute Werdnig-Hoffmann disease or spinal muscular atrophy Type I) is a distinct genetic and clinical entity. This has prom...

Journal: :Journal of dermatological case reports 2016
Jana Kyrova Lenka Kopeckova Hana Buckova Lenka Mrazova Karel Vesely Marketa Hermanova Hana Oslejskova Lenka Fajkusova

BACKGROUND Epidermolysis bullosa simplex associated with muscular dystrophy is a genetic skin disease caused by plectin deficiency. A case of a 19-year-old Czech patient affected with this disease and a review all previously published clinical cases are presented. MAIN OBSERVATIONS In our patient, skin signs of the disease developed after birth. Bilateral ptosis at the age of 8 years was cons...

شباهنگ, حسین , مداح, قدرت الله , نوقابی, رضا شریفی ,

Background: Hydatid disease or echinococcosis is a common parasitic disease of human and bovine, caused by infection with larva of the cestode echinococcus. Liver is the most common organ that is involved in this disease. Pelvic involvement and neurological symptoms, due to mass effect of pelvic involvement, in lower extremities are very uncommon manifestations of the disease.Case presentation:...

Journal: :acta medica iranica 0
bagher larijani endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran. ensieh nasli esfahani endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran. peyvand amini endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran. behrouz nikbin department of immunology, tehran university of medical sciences, tehran, iran. kamran alimoghaddam hematology-oncology & bmt research center, shariati hospital, tehran university of medical sciences, tehran, iran. somayeh amiri endocrinology and metabolism research center, tehran university of medical sciences, tehran, iran.

stem cells are undifferentiated cells with the ability of proliferation, regeneration, conversion to differentiated cells and producing various tissues. stem cells are divided into two categories of embryonic and adult. in another categorization stem cells are divided to totipotent, multipotent and unipotent cells. so far usage of stem cells in treatment of various blood diseases has been studi...

Journal: :Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition 2015
Jillian Davis Emily Samuels Lucille Mullins

Duchenne muscular dystrophy (DMD) is a serious degenerative muscular disease affecting males. Diagnosis usually occurs in childhood and is confirmed through genetic testing and/or muscle biopsy. Accompanying the disease are several nutrition-related concerns: growth, body composition, energy and protein requirements, constipation, swallowing difficulties, bone health, and complementary medicine...

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