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Protein S deficiency
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11	Haemophilia (2008), 14, 1214–1221 DOI: [removed]j[removed]01838.x ORIGINAL ARTICLE Add to Reading List Source URL: www.hemophilia.org Language: English - Date: 2014-04-22 11:47:02 Hematology Protein C deficiency Protein S deficiency Thrombophilia Coagulation Antiphospholipid syndrome Deep vein thrombosis Thrombin Antithrombin Blood Coagulation system Anatomy
12	Protein S deficiency: a clinical perspective Add to Reading List Source URL: www.hemophilia.org Language: English - Date: 2014-04-22 11:47:02 Anatomy Protein S deficiency Coagulation Activated protein C resistance Thrombophilia Thrombin Pulmonary embolism Antithrombin Deep vein thrombosis Blood Coagulation system Hematology
13	World Thrombosis Day Awareness Video Know the Signs and Symptoms of Patients with a Thrombosis: World Thrombosis Day For Health Care Professionals As health care providers, you know that thrombosis is the common disorde Add to Reading List Source URL: www.worldthrombosisday.org Language: English - Date: 2014-09-26 12:23:10 Deep vein thrombosis Thrombosis Pulmonary embolism Stroke Venous thrombosis Thrombus Preventive medicine Protein C deficiency Protein S deficiency Medicine Health Hematology
14	Phenylketonuria (PKU) What is Phenylketonuria? Phenylketonuria (also known as PKU) is an inherited condition that affects the way a person’s body uses protein. A person with PKU cannot use a component of protein called Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 15:48:27 Mental retardation Phenylketonuria PKU Phenylalanine Dominance Hyperphenylalanemia Medical genetics Newborn screening Tetrahydrobiopterin deficiency Medicine Health Biology
15	Diagnosis: Argininosuccinic Aciduria or Arginosuccinic Lyase Deficiency (ASA) ASA is an inherited disorder that limits the body’s ability to convert ammonia to urea. During periods of illness, fasting or protein overlo Add to Reading List Source URL: www.wadsworth.org Language: English - Date: 2009-07-15 13:48:21 Argininosuccinic aciduria Hyperammonemia Organic acidemia Carnitine Medical genetics Medicine Health Rare diseases
16	GUIDELINES FOR THE LABORATORY INVESTIGATION OF INHERITED THROMBOPHILIAS RECOMMENDATIONS FOR FIRST LEVEL CLINICAL LABORATORIES European Community Confederation of Clinical Chemistry (EC4) Working Group on Guidelines for I Add to Reading List Source URL: www.sibioc.it Language: English - Date: 2014-03-19 09:07:42 Coagulation system Thrombophilia Antiphospholipid syndrome Antithrombin Coagulation Protein S deficiency Protein C deficiency Thrombin Factor X Blood Medicine Hematology
17	Protein S deficiency: a clinical perspective Add to Reading List Source URL: www.stoptheclot.org Language: English - Date: 2014-03-19 16:45:31 Anatomy Protein S deficiency Coagulation Activated protein C resistance Thrombophilia Thrombin Pulmonary embolism Antithrombin Deep vein thrombosis Blood Coagulation system Hematology
18	Haemophilia (2008), 14, 1214–1221 DOI: [removed]j[removed]01838.x ORIGINAL ARTICLE Add to Reading List Source URL: www.stoptheclot.org Language: English - Date: 2014-03-19 16:45:31 Hematology Protein C deficiency Protein S deficiency Thrombophilia Coagulation Antiphospholipid syndrome Deep vein thrombosis Thrombin Antithrombin Blood Coagulation system Anatomy
19	Long-chain L-3-hydroxy acyl-CoA Dehydrogenase Deficiency (LCHAD) Trifunctional Protein Deficiency (TFP) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 10:42:23 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Newborn screening Mitochondrial trifunctional protein deficiency Fatty-acid metabolism disorder Mitochondrial trifunctional protein Health Medicine Rare diseases
20	Congenital Adrenal Hyperplasia (CAH) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel 24 to 36 hours after birth. The blood is tested for rare, hidden di Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 10:27:04 Medicine Intersexuality Congenital adrenal hyperplasia Newborn screening Steroidogenic acute regulatory protein Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Cytochrome P450 reductase Lipoid congenital adrenal hyperplasia Health Adrenal gland disorders Pediatrics