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NORD Physician Guides - NORD Physician Guides - Rare Disease Resources for Medical Professionals

Share with a Colleague. Homozygous Familial Hypercholesterolemia (HoFH). Lipoprotein Lipase Deficiency (LPLD). For additional information on over. 3,000 other rare diseases visit. NORD's Rare Disease Database. Lipoprotein Lipase Deficiency (LPLD). LPLD is a rare monogenic disorder of triglyceride metabolism. Deficiency of the enzyme lipoprotein lipase results in pronounced accumulation of triglycerides in the plasma. Homozygous Familial Hypercholesterolemia (HoFH). Welcome to the official rare disease ed...

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Share with a Colleague. Homozygous Familial Hypercholesterolemia (HoFH). Lipoprotein Lipase Deficiency (LPLD). For additional information on over. 3,000 other rare diseases visit. NORD's Rare Disease Database. Lipoprotein Lipase Deficiency (LPLD). LPLD is a rare monogenic disorder of triglyceride metabolism. Deficiency of the enzyme lipoprotein lipase results in pronounced accumulation of triglycerides in the plasma. Homozygous Familial Hypercholesterolemia (HoFH). Welcome to the official rare disease ed...

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NORD Physician Guides - NORD Physician Guides - Rare Disease Resources for Medical Professionals | nordphysicianguides.org Reviews

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Share with a Colleague. Homozygous Familial Hypercholesterolemia (HoFH). Lipoprotein Lipase Deficiency (LPLD). For additional information on over. 3,000 other rare diseases visit. NORD's Rare Disease Database. Lipoprotein Lipase Deficiency (LPLD). LPLD is a rare monogenic disorder of triglyceride metabolism. Deficiency of the enzyme lipoprotein lipase results in pronounced accumulation of triglycerides in the plasma. Homozygous Familial Hypercholesterolemia (HoFH). Welcome to the official rare disease ed...

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Pompe Disease - Introduction - NORD Physician Guides - Rare Disease Resources for Medical Professionals

http://nordphysicianguides.org/pompe-disease

Share with a Colleague. GLYCOGEN STORAGE DISEASE, TYPE II; ACID MALTASE DEFICIENCY). In 1995 at the age of twelve, Tiffany House was diagnosed with Pompe disease, a rare, progressive, metabolic disorder. At that time, her parents were told that there was no treatment or cure for Pompe disease and that Tiffany probably would not live beyond her second decade. This guide is part of a series on rare diseases provided by NORD, free of charge, to medical professionals in the hope of encouraging early recognit...

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Hereditary Angioedema - NORD Physician Guides - Rare Disease Resources for Medical Professionals

http://nordphysicianguides.org/hereditary-angioedema

Share with a Colleague. Sign up for updates:. Follow NORD News here. For Email Newsletters you can trust. Index of Physician Guides. Share with a Colleague. For Patients and Families. NORD is a unique federation of individuals and voluntary health organizations dedicated to helping people with rare diseases and assisting the organizations that serve them. NORD is committed to the identification, treatment and cure of rare diseases through programs of education, advocacy, research, and patient services.

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Infantile Spasms - Introduction - NORD Physician Guides - Rare Disease Resources for Medical Professionals

http://nordphysicianguides.org/infantile-spasms

Share with a Colleague. Welcome to the NORD Physician Guide to Infantile Spasms. By Cristina Y. Go, MD,. And O Carter Snead III, MD, FAAN. The authors are members of the Department of Neurology, Hospital for Sick Children, Toronto, Canada. Infantile spasms is a catastrophic epilepsy syndrome with onset in the first year of life. Prompt diagnosis and urgent treatment of affected children can improve their long-term outcomes. Infantile spasms is characterized clinically by epileptic spasms which consist of...

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Myelofibrosis - Introduction - NORD Physician Guides - Rare Disease Resources for Medical Professionals

http://nordphysicianguides.org/myelofibrosis

Share with a Colleague. Welcome to the NORD Physician Guide to Myelofibrosis. The NORD Online Physician Guides are written for physicians by physicians with expertise on specific rare disorders. This guide was written by John Mascarenhas, MD. Of Mount Sinai School of Medicine (see acknowledgements for additional information). Myelofibrosis (MF) is categorized as a chronic myeloproliferative neoplasm (MPN). This is a group of heterogeneous, hematopoietic stem-cell malignancies. Symptoms & Signs. Share wit...

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Amyloidosis - NORD Physician Guides - Rare Disease Resources for Medical Professionals

http://nordphysicianguides.org/amyloidosis

Share with a Colleague. Amyloidosis is a systemic disorder characterized by the extracellular deposition of a protein-like material in multiple organs. The deposition of amyloid leads to progressive organ dysfunction. There are several types of amyloidosis, and they are classified according to their precursor protein. Sign up for updates:. Follow NORD News here. For Email Newsletters you can trust. Index of Physician Guides. Share with a Colleague. For Patients and Families.

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I am a passionate web developer with over 14 years of experience. Consultant and Freelance Web Developer and Webmaster { speckz.com. Self Employed } Oct 2007 Present. Worked with clients and teams to complete the following websites:. Emunah of America WordPress site maintenance and support for online donations and e-commerce via GiveWP and WooCommerce emunah.org. Physician Guide nordphysicianguides.org. Rare Disease Day USA rarediseaseday.us. RareDisease Dialog Blog blog.rarediseases.org. StyleHaul AWS H...

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Hereditary Angioedema HAE Resources Berinert USHAA Cinryze C1 Esterase Inhibitor - BioRx

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Join Our Mailing List. Hereditary Angioedema (HAE) Resources. US Hereditary Angioedema Association. International Patient Organization for C1 Inhibitor Deficiencies). National Organization for Rare Disorders. Berinert (C1 Esterase Inhibitor [Human]). National Organization for Rare Disorders. National Library of Medicine. 7167 E. Kemper Road. Cincinnati, OH 45249. If you’d like to make a referral, please complete our referral form. Can I Use BioRX?

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nordphysicianguides.org

NORD Physician Guides - NORD Physician Guides - Rare Disease Resources for Medical Professionals

Share with a Colleague. Homozygous Familial Hypercholesterolemia (HoFH). Lipoprotein Lipase Deficiency (LPLD). For additional information on over. 3,000 other rare diseases visit. NORD's Rare Disease Database. Lipoprotein Lipase Deficiency (LPLD). LPLD is a rare monogenic disorder of triglyceride metabolism. Deficiency of the enzyme lipoprotein lipase results in pronounced accumulation of triglycerides in the plasma. Homozygous Familial Hypercholesterolemia (HoFH). Welcome to the official rare disease ed...

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NORD Physician Guides - NORD Physician Guides - Rare Disease Resources for Medical Professionals

Share with a Colleague. Homozygous Familial Hypercholesterolemia (HoFH). Lipoprotein Lipase Deficiency (LPLD). For additional information on over. 3,000 other rare diseases visit. NORD's Rare Disease Database. Lipoprotein Lipase Deficiency (LPLD). LPLD is a rare monogenic disorder of triglyceride metabolism. Deficiency of the enzyme lipoprotein lipase results in pronounced accumulation of triglycerides in the plasma. Homozygous Familial Hypercholesterolemia (HoFH). Welcome to the official rare disease ed...

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