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Hypophosphatasia
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1	Strensiq, INN-asfotase alfa Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2016-01-29 11:52:49 Chemistry Recombinant proteins Medicine Clinical medicine Sodium channel blockers Diabetes Insulin aspart Alcohols Asfotase alfa Hypophosphatasia Lorazepam
2	Department of Molecular Genetics Massively Parallel Sequencing for Brittle Bone Disorders and Hereditary Rickets Osteogenesis imperfecta (OI) comprises a group of inherited disorders characterized by bone fragility and Add to Reading List Source URL: www.anzbms.org.au Language: English - Date: 2015-04-08 23:11:01 Rare diseases Collagen disease Molecular biology DNA sequencing Collagen type I alpha 1 X-linked hypophosphatemia Leprecan Osteogenesis imperfecta Hypophosphatasia Biology Health Genetics
3	Product Datasheet Anti-Alkaline Phosphatase, Tissue Non-Specific antibody [EPR4477] ab108337 1 Abreviews Add to Reading List Source URL: www.abcam.com Language: English Staining Laboratory techniques Immune system Protein methods Immunohistochemistry Alkaline phosphatase ALPL Antibody Hypophosphatasia Anatomy Biology Immunologic tests
4	PDF Document Add to Reading List Source URL: www.kennedykrieger.org Language: English - Date: 2013-12-31 08:49:41 Collagen disease Osteogenesis imperfecta Collagen type I alpha 1 Collagen Dentinogenesis imperfecta Teriparatide COL1A2 Osteoporosis Hypophosphatasia Anatomy Medicine Health
5	The Bone Center at Kennedy Krieger Institute Who We Are Add to Reading List Source URL: www.kennedykrieger.org Language: English - Date: 2013-12-31 08:49:46 Rare diseases Endocrine diseases Johns Hopkins University Kennedy Krieger Institute Osteoporosis Osteocalcin Teriparatide Hypophosphatasia Spinal cord injury Medicine Health Osteopathies
6	Frequently Asked Questions 1. If no members of my family are affected by OI, can I still have a child with the condition? Yes. Most infants with severe forms of OI are born into families with no history of OI. The cause Add to Reading List Source URL: www.mrds.org.my Language: English - Date: 2011-03-08 01:10:09 Biology Medical genetics Osteogenesis imperfecta Collagen type I alpha 1 Genetic disorder Dentinogenesis imperfecta Bone fracture Genetic testing Hypophosphatasia Medicine Genetics Collagen disease
7	Chemerin activates fibroblast-like synoviocytes in patients with rheumatoid arthritis Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Genetic genealogy Arthritis Molecular biology Chondrocalcinosis Single-nucleotide polymorphism International HapMap Project Genotyping Hypophosphatasia Haplotype Genetics Biology Population genetics
8	PDF Document Add to Reading List Source URL: medind.nic.in Language: English - Date: 2004-07-05 14:30:00 Developmental biology Anencephaly Hypophosphatasia Hydrocephalus Aplasia cutis congenita Acalvaria Cowasji Jehangir Cranial cavity Congenital disorder Health Acrania Rare diseases
9	PDF Document Add to Reading List Source URL: files.shareholder.com Language: English Rare diseases Alexion Pharmaceuticals Eculizumab Paroxysmal nocturnal hemoglobinuria Hemolytic-uremic syndrome Myasthenia gravis Hypophosphatasia Nephrology Health Medicine Acquired hemolytic anemia