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Muscle dystrophy
LE WE PMID CA
Muscle dystrophy1868Muskeldystrophie

Dystroglycan

Emerin

Emery Dreifuss dystrophy

Fukuyama congenital muscle dystrophy

Galgt2

Halofuginone

Histone deacetylase

Lamin

LARGE

Muscle dystrophy

Muscle eye brain disease

POMGnT1

POMT1

POMT2

Walker Warburg syndrome

1998  
1
The muscular dystrophies.
[9765171] BMJ 317(7164): 991-5 (1998)
2008  
2
Cardiac involvement in muscular dystrophies.
[18238819] QJM 101(5): 337-44 (2008)
2005  
3
The D4Z4 repeat-mediated pathogenesis of facioscapulohumeral muscular dystrophy.
[15674778] Am J Hum Genet 76(3): 375-86 (2005)
1992  
4
Recent advances in understanding muscular dystrophy.
[1444538] Arch Dis Child 67(10): 1310-2 (1992)
2004  
5
The congenital and limb-girdle muscular dystrophies: sharpening the focus, blurring the boundaries.
[14967765] Arch Neurol 61(2): 189-99 (2004)
2007  
6
Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A.
[18055493] Brain 130(Pt 12): 3237-49 (2007)
1999  
7
Making sense of the limb-girdle muscular dystrophies.
[10430828] Brain 122 ( Pt 8)(-): 1403-20 (1999)
2003  
8
Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations.
[14659775] Eur Heart J 24(24): 2227-36 (2003)
2006  
9
Ventilatory assistance in patients with Duchenne muscular dystrophy.
[16946091] Eur Respir J 28(3): 468-9 (2006)
1992  
10
Report of ENMC workshop on the limb-girdle muscular dystrophies.
[1359146] J Med Genet 29(10): 753-5 (1992)
2005  
11
Cardiovascular health supervision for individuals affected by Duchenne or Becker muscular dystrophy.
[16322188] Pediatrics 116(6): 1569-73 (2005)
1992  
12
2007  
13
Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.
[18646565] Acta Myol 26(3): 159-64 (2007)
2007  
14
Muscular dystrophies due to defective glycosylation of dystroglycan.
[18646561] Acta Myol 26(3): 129-35 (2007)
2004  
15
Muscular dystrophy: from pathogenesis to strategy.
[15478675] Acta Neurol Taiwan 13(2): 50-8 (2004)
2009  
16
Congenital muscular dystrophy. Part I: a review of phenotypical and diagnostic aspects.
[19330236] Arq Neuropsiquiatr 67(1): 144-68 (2009)
2009  
17
Congenital muscular dystrophy. Part II: a review of pathogenesis and therapeutic perspectives.
[19547838] Arq Neuropsiquiatr 67(2A): 343-62 (2009)
2008  
18
Focusing on fibrosis: halofuginone-induced functional improvement in the mdx mouse model of Duchenne muscular dystrophy.
[18310507] Am J Physiol Heart Circ Physiol 294(4): H1505-7 (2008)
2009  
19
Adherence to american academy of pediatrics recommendations for cardiac care among female carriers of duchenne and becker muscular dystrophy.
[19254982] Pediatrics 123(3): e471-5 (2009)
2010  
20
Limb-girdle muscular dystrophy type 2A.
[20739783] Neurol India 58(4): 509-11 (2010)
2008  
21
A brief history of muscular dystrophy research: a personal perspective.
[18974548] Neurol India 56(3): 231-5 (2008)
2008  
22
How to go about diagnosing and managing the limb-girdle muscular dystrophies.
[18974553] Neurol India 56(3): 271-80 (2008)
2008  
23
Limb girdle muscular dystrophies in India.
[18974554] Neurol India 56(3): 281-8 (2008)
2011  
24
Histone deacetylase inhibitors in the treatment of muscular dystrophies: epigenetic drugs for genetic diseases.
[21308150] Mol Med 17(5-6): 457-65 (2011)
2008  
25
Transient receptor potential cation channels in normal and dystrophic mdx muscle.
[18504127] Neuromuscul Disord 18(6): 501-13 (2008)
2005  
26
The muscular dystrophies: from genes to therapies.
[16305275] Phys Ther 85(12): 1372-88 (2005)
2006  
27
The congenital muscular dystrophies: recent advances and molecular insights.
[17163796] Pediatr Dev Pathol 9(6): 427-43 (2006)
2010  
28
Therapeutic targeting of signaling pathways in muscular dystrophy.
[19816663] J Mol Med (Berl) 88(2): 155-66 (2010)
2007  
29
Congenital muscular dystrophies involving the O-mannose pathway.
[17584082] Curr Mol Med 7(4): 417-25 (2007)

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