نتایج جستجو برای: muscular

تعداد نتایج: 43642  

Journal: :Brain : a journal of neurology 2012
Emily C Oates Stephen Reddel Michael L Rodriguez Luke C Gandolfo Melanie Bahlo Simon H Hawke Shireen R Lamandé Nigel F Clarke Kathryn N North

Autosomal dominant congenital spinal muscular atrophy is characterized by predominantly lower limb weakness and wasting, and congenital or early-onset contractures of the hip, knee and ankle. Mutations in TRPV4, encoding a cation channel, have recently been identified in one large dominant congenital spinal muscular atrophy kindred, but the genetic basis of dominant congenital spinal muscular a...

Background: The association of limb-girdle muscular dystrophy (LGMD) with other neurological disorders is uncommon. Case presentation: We report a 25-year-old female with LGMD who suffered from slowly progressive proximal muscular weakness and atrophy since she was 12 years of age. The patient recently presented with acute loss of left side visual acuity. After evaluation, findings were sugges...

Journal: :Journal of medical genetics 1989
G K Suthers J I Manson L M Stern E A Haan J C Mulley

We describe a man with Becker muscular dystrophy whose weakness was minimal in contrast to that of his more severely affected nephews. This man had a Klinefelter karyotype (47,XXY) and his mild symptoms may be attributed to him being heterozygous for the muscular dystrophy gene. This is the first report of a person with both Klinefelter's syndrome and Becker muscular dystrophy. This combination...

2010
Murat Sensoy

Cite as: O " " ? B ! ! m " ' Proc. of 9th Int. Conf. on Autonomous Agents and Multiagent Systems (AAMAS 2010) # $ $ % $ " & ! ' ()*(+ ,)() . / & / ' © ,)() ! "' 000& & & & g !N (& The search interest “Comedy Videos that contain a muscular guy who is chased by a small dog” can be represented as Comedy Video ∃ contain.(Small Dog ∃ chase.(Muscular Man)). On the other hand, the search interest “Com...

2006
A. MOOSA V. DUBOWITZ

Moosa, A., and Dubowitz, V. (1973). Archives of Disease in Childhood, 48, 386. Spinal muscular atrophy in childhood: two clues to clinical diagnosis. A coarse tremor was noted in 13 children suffering from the childhood form of spinal muscular atrophy. Tremor has not been seen in any other condition producing proximal muscle weakness in childhood, and its presence should therefore suggest the d...

Journal: :Seminars in respiratory and critical care medicine 2002
Anita K Simonds

Pulmonary complications including chest infections, atelectasis, pulmonary hypoplasia and ventilatory failure are the leading cause of death in the muscular dystrophies and atrophies. Ventilatory insufficiency is virtually inevitable in Duchenne muscular dystrophy and type 1 spinal muscular atrophy (SMA), but more variable in limb-girdle, congenital, and facioscapulohumeral muscular dystrophy. ...

Journal: :iranian journal of public health 0
ayuni nabilah alias karmegam karuppiah shamsul bahri mohd tamrin emilia zainal abidin umi kalsom mohd shafie sivasankar sambasivam

background: motorcycle has been one of the vital modes of transportation worldwide. it is quite difficult to identify the risk factors that affect muscular discomfort among motorcyclist due to not much research having been carried out on the motorcyclist. the purpose of this study was to have a better understanding of the risk factors of muscular discomfort among motorcyclist due to motorcycle ...

Journal: :genetics in the 3rd millennium 0
sirous zeinali marziyeh mojbafan hamideh bagherian elham davoodi

limb girdle muscular dystrophies (lgmds) are group of neuromuscular disorders which are characterized by progressive muscle weakness and they mostly affect the pelvic and shoulder girdle muscles. this disease can be inherited as autosomal dominant (lgmd1) and autosomal recessive (lgmd2). so far seven autosomal dominant and 20 autosomal recessive forms of this disease have been recognized reflec...

Journal: :journal of dental materials and techniques 0
majid majid eshghpour dental research center, department of oral and maxillofacial surgery, faculty of dentistry, mashhad university of medical sciences, mashhad, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) baratolah baratolah shaban dental research center, department of oral and maxillofacial surgery, faculty of dentistry, mashhad university of medical sciences, mashhad, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) reza reza shahakbari dental material research center, department of oral and maxillofacial surgery, faculty of dentistry, mashhad university of medical sciences, mashhad, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) reza reza mahvelati shamsabadi department of orthodontics, hamedan university of medical sciences, hamedan, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی همدان (hamadan university of medical sciences) amir hossein amir hossein nejat general dentist, mashhad, iran

introduction: bilateral sagittal split osteotomy (bsso) of mandible is vastly used in treatment of mandibular deficiencies and discrepancies. since this method could affect esthetic as well as function, evaluating these effects from various aspects is crucial. this study assessed the effects of this technique on the function of masseter muscle, jaw movements, and sensory changes along with fail...

2015
Gustavo Torres de Souza Rafaella de Souza Salomão Zanette Danielle Luciana Aurora Soares do Amaral Francisco Carlos da Guia Claudinéia Pereira Maranduba Camila Maurmann de Souza Ernesto da Silveira Goulart Guimarães João Vitor Paes Rettore Natana Chaves Rabelo Antônio Márcio Resende do Carmo Fernando de Sá Silva Carlos Magno da Costa Maranduba

The satellite cells are long regarded as heterogeneous cell population, which is intimately linked to the processes of muscular recovery. The heterogeneous cell population may be classified by specific markers. In spite of the significant amount of variation amongst the satellite cell populations, it seems that their activity is tightly bound to the paired box 7 transcription factor expression,...

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