Platelet m-calpain: a facile marker and STR polymorphism analysis for the identification of true carriers of Duchenne muscular dystrophy

V. Mohana Rao; K. Sridevi; M. P. J. S. Anandraj

doi:10.1039/c1ib00101a

Platelet m-calpain: a facile marker and STR polymorphism analysis for the identification of true carriers of Duchenne muscular dystrophy

Integrative Biology ◽

10.1039/c1ib00101a ◽

2011 ◽

Vol 4 (2) ◽

pp. 202-208

Author(s):

V. Mohana Rao ◽

K. Sridevi ◽

M. P. J. S. Anandraj

Keyword(s):

Duchenne Muscular Dystrophy ◽

Muscular Dystrophy ◽

Polymorphism Analysis ◽

Str Polymorphism

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Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy by restriction fragment length polymorphism analysis with pERT 87 deoxyribonucleic acid probes

American Journal of Obstetrics and Gynecology ◽

10.1016/0002-9378(88)90023-3 ◽

1988 ◽

Vol 158 (3) ◽

pp. 548-555 ◽

Cited By ~ 6

Author(s):

Susumu Katayama ◽

Monty Montano ◽

R.Nathan Slotnick ◽

Roger V. Lebo ◽

Mitchell S. Golbus

Keyword(s):

Prenatal Diagnosis ◽

Duchenne Muscular Dystrophy ◽

Muscular Dystrophy ◽

Restriction Fragment Length Polymorphism ◽

Length Polymorphism ◽

Fragment Length ◽

Deoxyribonucleic Acid ◽

Fragment Length Polymorphism ◽

Polymorphism Analysis ◽

Restriction Fragment Length

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Determination of Duchenne muscular dystrophy carrier status by single strand conformation polymorphism analysis of deleted regions of the dystrophin locus.

Journal of Medical Genetics ◽

10.1136/jmg.28.12.856 ◽

1991 ◽

Vol 28 (12) ◽

pp. 856-859 ◽

Cited By ~ 4

Author(s):

R I Richards ◽

K Friend

Keyword(s):

Duchenne Muscular Dystrophy ◽

Muscular Dystrophy ◽

Single Strand Conformation Polymorphism ◽

Single Strand ◽

Carrier Status ◽

Polymorphism Analysis ◽

Conformation Polymorphism Analysis ◽

Conformation Polymorphism

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Use of cyanuric chloride-activated paper for detection of subpicogram quantities of specific DNA sequences and its application to linked restriction fragment length polymorphism analysis in a Duchenne muscular dystrophy affected family

Analytical Biochemistry ◽

10.1016/0003-2697(87)90199-0 ◽

1987 ◽

Vol 165 (1) ◽

pp. 45-55 ◽

Cited By ~ 2

Author(s):

H.-D. Hunger ◽

A. Speer ◽

Chr. Flachmeier ◽

R. Hanke ◽

G. Behrendt ◽

...

Keyword(s):

Duchenne Muscular Dystrophy ◽

Muscular Dystrophy ◽

Restriction Fragment Length Polymorphism ◽

Restriction Fragment ◽

Length Polymorphism ◽

Dna Sequences ◽

Fragment Length ◽

Fragment Length Polymorphism ◽

Polymorphism Analysis ◽

Restriction Fragment Length

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Impact of Bisphosphonates on Survival for Patients With Duchenne Muscular Dystrophy

Yearbook of Neurology and Neurosurgery ◽

10.1016/j.yneu.2011.04.066 ◽

2011 ◽

Vol 2011 ◽

pp. 198-199

Author(s):

G.N. Breningstall

Keyword(s):

Duchenne Muscular Dystrophy ◽

Muscular Dystrophy

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Treatment of Duchenne muscular dystrophy with cyclosporin A – A randomized, double-blind, placebo controlled trial

Neuropediatrics ◽

10.1055/s-0029-1215757 ◽

2008 ◽

Vol 39 (05) ◽

Author(s):

J Kirschner ◽

J Schessl ◽

G Ihorst ◽

R Korinthenberg

Keyword(s):

Duchenne Muscular Dystrophy ◽

Muscular Dystrophy ◽

Cyclosporin A ◽

Controlled Trial ◽

Double Blind ◽

Double Blind Placebo

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Health- related quality of life in patients with Duchenne Muscular Dystrophy

Neuropediatrics ◽

10.1055/s-0031-1273950 ◽

2011 ◽

Vol 42 (S 01) ◽

Cited By ~ 1

Author(s):

B Geers ◽

S Elsenbruch ◽

J Schmid ◽

U Schara

Keyword(s):

Quality Of Life ◽

Duchenne Muscular Dystrophy ◽

Muscular Dystrophy ◽

Health Related Quality ◽

Related Quality ◽

Health Related

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Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy

Neuropediatrics ◽

10.1055/s-0031-1274094 ◽

2011 ◽

Vol 42 (S 01) ◽

Author(s):

M von der Hagen ◽

M Smitka ◽

A Pyper ◽

M Breiting ◽

A Müller ◽

...

Keyword(s):

Palliative Care ◽

Duchenne Muscular Dystrophy ◽

Muscular Dystrophy ◽

Spinal Muscular Atrophy ◽

Muscular Atrophy ◽

Neuromuscular Disorders ◽

Pediatric Palliative Care ◽

Type I ◽

Spinal Muscular Atrophy Type ◽

Life Threatening

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Growth and psychomotor development of patients with Duchenne Muscular Dystrophy

Neuropediatrics ◽

10.1055/s-0032-1307138 ◽

2012 ◽

Vol 43 (02) ◽

Author(s):

E Sarrazin ◽

M von der Hagen ◽

U Schara ◽

K von Au ◽

A Kaindl

Keyword(s):

Duchenne Muscular Dystrophy ◽

Muscular Dystrophy ◽

Psychomotor Development

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Current care practice in Duchenne muscular dystrophy in Europe - results of the CARE-NMD cross-sectional survey

Neuropediatrics ◽

10.1055/s-0033-1337747 ◽

2013 ◽

Vol 44 (02) ◽

Cited By ~ 1

Author(s):

J Vry ◽

K Gramsch ◽

K Bushby ◽

H Lochmüller ◽

S Rodger ◽

...

Keyword(s):

Duchenne Muscular Dystrophy ◽

Muscular Dystrophy ◽

Care Practice ◽

Cross Sectional Survey ◽

Cross Sectional

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Use of Complementary and Alternative Medicine (CAM) in Patients with X-Linked Recessive Duchenne Muscular Dystrophy (DMD)

Neuropediatrics ◽

10.1055/s-0036-1583655 ◽

2016 ◽

Vol 47 (S 01) ◽

Author(s):

E. Giagkou ◽

T. Zuzak ◽

U. Schara

Keyword(s):

Duchenne Muscular Dystrophy ◽

Muscular Dystrophy ◽

Alternative Medicine ◽

Complementary And Alternative Medicine ◽

Complementary And Alternative

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