Alpha acid

Results: 438



#Item
221Genetic genealogy / BioMarin Pharmaceutical / Glycogen storage disease type II / Acid alpha-glucosidase / Lysosomal storage disease / Mucopolysaccharidosis / Alglucosidase alfa / Neuronal ceroid lipofuscinosis / Tetrahydrobiopterin / Health / Rare diseases / Medicine

Contact: Investors: Traci McCarty BioMarin Pharmaceutical Inc[removed]

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Source URL: amdapompe.ehclients.com

Language: English - Date: 2014-06-08 18:46:42
222Rare 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

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,

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Source URL: amdapompe.ehclients.com

Language: English - Date: 2010-04-02 02:44:57
223Motor neurone disease / Glycogen storage disease type II / Hepatology / Lysosomal storage disease / Dysphagia / Swallowing / Acid alpha-glucosidase / Amyotrophic lateral sclerosis / Hypotonia / Health / Medicine / Rare diseases

J Inherit Metab Dis DOI[removed]s10545[removed]ORIGINAL ARTICLE Facial-muscle weakness, speech disorders and dysphagia

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Source URL: amdapompe.ehclients.com

Language: English - Date: 2012-01-17 11:57:59
224Knowledge / Glycogen storage disease type II / Rasch model / Item response theory / Patient-reported outcome / Scale / Acid alpha-glucosidase / Rasch / Level of measurement / Psychometrics / Statistics / Education

ARTICLE IN PRESS Available online at www.sciencedirect.com Neuromuscular Disorders xxx[removed]xxx–xxx www.elsevier.com/locate/nmd

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Source URL: amdapompe.ehclients.com

Language: English - Date: 2013-08-24 22:47:13
225Rare diseases / Nociception / Glycogen storage disease type II / Hepatology / Acid alpha-glucosidase / Fabry disease / Lysosomal storage disease / Chronic pain / Medicine / Health / Pain

Pain in adult patients with Pompe disease

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Source URL: amdapompe.ehclients.com

Language: English - Date: 2013-08-24 22:34:38
226Matter / Cooking oils / Fatty acids / Nutrition / Lipids / Vegetable fats and oils / Smoke point / Alpha-Linolenic acid / Grape seed oil / Soft matter / Vegetable oils / Food and drink

TM[removed]COOKING Using the Right Oil for the Right Reasons Where there’s smoke there’s fire! You’re chopping garlic when you notice smoke rising from the cooking oil you’ve been heating in the

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Source URL: www.ebnaturalmedicine.com

Language: English - Date: 2014-06-23 23:53:05
227Inborn errors of carbohydrate metabolism / Rare diseases / Glycogen storage disease type II / Lysosomal storage disease / Acid alpha-glucosidase / Enzyme replacement therapy / Glycogen / Medicine / Health / Hepatology

NIH Public Access Author Manuscript Neurotherapeutics. Author manuscript; available in PMC 2009 October 14. NIH-PA Author Manuscript

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Source URL: amdapompe.ehclients.com

Language: English - Date: 2010-07-21 23:05:58
228Immune system / Immunology / Glycoproteins / Applied genetics / Biotechnology / Adeno-associated virus / Glycogen storage disease type II / Acid alpha-glucosidase / Gene therapy / Biology / Medicine / Health

Immunomodulatory Gene Therapy Prevents Antibody Formation and Lethal Hypersensitivity Reactions in Murine Pompe Disease

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Source URL: amdapompe.ehclients.com

Language: English - Date: 2011-06-05 23:30:36
229Neurological disorders / Glycogen storage disease type II / Hepatology / Cancer-related fatigue / Lysosomal storage disease / Fatigue / Enzyme replacement therapy / Chronic fatigue syndrome / Acid alpha-glucosidase / Health / Medicine / Rare diseases

Enzyme replacement therapy and fatigue in adults with Pompe disease

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Source URL: amdapompe.ehclients.com

Language: English - Date: 2013-08-24 22:32:07
230Gene delivery / Emerging technologies / Molecular biology / Applied genetics / Biotechnology / Glycogen storage disease type II / Acid alpha-glucosidase / Gene therapy / Lysosomal storage disease / Biology / Medicine / Health

HMG Advance Access published May 4, 2011 Human Molecular Genetics, 2011 doi:[removed]hmg/ddr174 R1–R8

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Source URL: amdapompe.ehclients.com

Language: English - Date: 2011-05-07 23:33:11
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