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Muscular dystrophy
Results: 605

#	Item
331	New hope in fight against muscular dystrophy Add to Reading List Source URL: medicalxpress.com Language: English - Date: 2014-11-26 06:22:56 Cytoskeleton Health Dystrophin Duchenne muscular dystrophy Sarcospan Dystrophin-associated protein complex Muscular dystrophy Biology Cell biology
332	¡Contraatacamos! Seis décadas de progreso contra la esclerosis lateral amiotrófica, conocida como la enfermedad de Lou Gehrig. MDA (Muscular Dystrophy Association) ayuda más a los pacientes de esa enfermedad, que otr Add to Reading List Source URL: mda.org Language: Spanish - Date: 2014-08-21 11:17:19
333	Lachmann and Schoser Orphanet Journal of Rare Diseases 2013, 8:160 http://www.ojrd.com/content[removed]REVIEW Open Access Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2014-02-22 17:47:38 Respiratory therapy Pulmonary function testing Respiratory physiology Clinical research Glycogen storage disease type II Lysosomal storage disease Spirometry Idiopathic pulmonary fibrosis Duchenne muscular dystrophy Medicine Health Pulmonology
334	Hindawi Publishing Corporation Case Reports in Medicine Volume 2009, Article ID[removed], 4 pages doi:[removed][removed]Case Report Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-07-21 22:30:08 Medicine Glycogen storage disease type II Whole body vibration Strength training Muscle Physical strength Duchenne muscular dystrophy Creatine Galileo Exercise Health Anatomy
335	ARTICLE The angiotensin-converting enzyme insertion/deletion polymorphism modifies the clinical outcome in patients with Pompe disease Paola de Filippi, PhD1, Sabrina Ravaglia, MD, PhD2, Bruno Bembi, MD3, Alfredo Costa, Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-04-02 02:44:57 Rare diseases Genetic genealogy Hepatology Genetics Glycogen storage disease type II Glycogen storage disease type V Lysosomal storage disease Acid alpha-glucosidase Duchenne muscular dystrophy Health Inborn errors of carbohydrate metabolism Medicine
336	EXPANDING THE PHENOTYPE OF LATE-ONSET POMPE DISEASE: TONGUE WEAKNESS: A NEW CLINICAL OBSERVATION ALBERTO DUBROVSKY, MD,1 JOSE CORDERI, PhT,1 MIN LIN, PhD,2 PRIYA S. KISHNANI, MBBS, MD,3 and HARRISON N. JONES, PhD4 1 Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-09-30 19:07:13 Motor neurone disease Glycogen storage disease type II Hepatology Amyotrophic lateral sclerosis Stroke Swallowing Muscular dystrophy Ptosis Myasthenia gravis Health Rare diseases Medicine
337	"DUB.ZPMPHJDBt999Q EDITORIAL Early is better? A new algorithm for early diagnosis Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2014-02-22 17:32:25** Lysosomal storage diseases Inborn errors of carbohydrate metabolism Glycogen storage disease type II Hepatology Acid alpha-glucosidase Limb-girdle muscular dystrophy Muscular dystrophy Amyotrophic lateral sclerosis Health Rare diseases Medicine
338	Standard of Care in Spinal Muscular Atrophy: A Consensus Statement by the International SMA Standard of Care Committee Add to Reading List Source URL: mdausa.org Language: English - Date: 2012-06-13 15:35:40 Spinal muscular atrophies SMN1 Hypotonia Muscular dystrophy Amyotrophic lateral sclerosis Muscle atrophy Scoliosis Neuromuscular Disorders Atrophy Medicine Health Motor neurone disease
339	The Emory ALS Center is designed and dedicated to performing cutting edge research while providing comprehensive care for people and families with ALS and related motor neuron diseases. Emory is recognized nationally as Add to Reading List Source URL: neurology.emory.edu Language: English - Date: 2013-05-23 15:24:49 Amyotrophic lateral sclerosis Motor neurone disease Muscular Dystrophy Association Neuroscience ALS Society of Canada ALS Therapy Development Institute Rare diseases Health ALS Association
340	amda AMDA Conference Call Transcript Session No. 7: Gene Therapy Speaker: Dr. Barry Byrne Date: Tuesday, August 31, 2004 Paul Kessler and I began to study the approach to treating inherited muscles diseases and we Add to Reading List Source URL: amda-pompe.org Language: English - Date: 2009-12-27 08:00:41 Rare diseases Molecular biology Gene delivery Muscular dystrophy Medical genetics Limb-girdle muscular dystrophy Gene therapy Myostatin Amyotrophic lateral sclerosis Biology Health Medicine

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