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2004, ISBN 0198508786, xxvii. 447
Lysosomal storage diseases are inherited metabolic disorders characterized by severe pathology, typically involving the brain. Although individually rare, they... 
Brain | Lysosomal storage diseases | Treatment | Metabolism | Disorders | neuroscience | Lysosomal storage disorders - Treatment
Book
2009, 1, ISBN 140516915X, ix, 192
The first book with a holistic approach to all aspects of care for women with inherited bleeding disorders Ever wondered about heavy menstrual bleeding that... 
Hematology | MEDICAL | Women | Blood coagulation disorders in pregnancy | Blood coagulation disorders | Diseases
Book
2006, ISBN 9781588295590, xvii, 426
A grand summary and synthesis of the tremendous amount of data now available in the post genomic era on the structural features, architecture, and evolution of... 
Other branches of medicine | Genetic disorders | Molecular aspects | Diseases | Medicine & Public Health | Pathology
Book
2006, 5th ed., ISBN 0781749964, 400
Recommended in the Brandon-Hill selected list of print books and journals for the small medical library - April 2003, the pre-eminent reference on coagulation... 
Blood Coagulation Disorders | Hemostasis | Thrombosis | Hemorrhagic Disorders
eBook
2010, 1, Series for the International Neuropsychological Society, ISBN 9780521685368, xvi, 220
Genetic syndromes and neurodevelopmental disorders that have a genetic basis are associated with cognitive and academic disabilities. Genes, Brain and... 
Neurologic manifestations of general diseases | Genetic aspects | Genetic disorders | Developmental disabilities | Psychophysiology
Book
Haematologica, ISSN 0390-6078, 03/2007, Volume 92, Issue 3, pp. 357 - 365
Departments of Clinical Laboratory (TQ, MG); Hematology-Oncology (OP, EA, CM, SB, BM, PZ, JP, DM) School of Medicine, Pontificia Universidad Católica de Chile... 
Mucous and skin bleeding | Relative frequency of disorders of primary hemostasis | Diagnosis of inherited disorders of primary hemostasis | Platelet function study | Bleeding of unknown cause | Mild bleeding disorders | STORAGE POOL DEFICIENCY | DIAGNOSIS | bleeding of unknown cause | diagnosis of inherited disorders of primary hemostasis | PLATELET-FUNCTION | DISORDERS | mild bleeding disorders | TIME | mucous and skin bleeding | VON-WILLEBRAND-DISEASE | BRUISING SYMPTOMATOLOGY | FACTOR-XI | platelet function study | relative frequency of disorders of primary hemostasis | TYPE-1 | HEMATOLOGY | ABO BLOOD-GROUP | Medical History Taking | Predictive Value of Tests | Prevalence | Prospective Studies | Humans | Middle Aged | Child, Preschool | Hemorrhagic Disorders - blood | Male | von Willebrand Diseases - complications | Blood Platelet Disorders - complications | Hemorrhagic Disorders - genetics | Bleeding Time | Child | Platelet Function Tests - methods | Signal Transduction | Coagulation Protein Disorders - blood | Hemorrhage - blood | Coagulation Protein Disorders - complications | Phenotype | Case Management | Blood Platelets - metabolism | Spain - epidemiology | Adolescent | Platelet Function Tests - instrumentation | Hemorrhagic Disorders - diagnosis | Hemorrhagic Disorders - epidemiology | von Willebrand Diseases - blood | von Willebrand Diseases - epidemiology | Mucous Membrane | Blood Platelet Disorders - blood | Case-Control Studies | Hemorrhagic Disorders - complications | Hemorrhage - etiology | Adult | Female | Surveys and Questionnaires | von Willebrand Diseases - classification | Blood Platelets - drug effects | Severity of Illness Index | Blood Platelet Disorders - epidemiology | Coagulation Protein Disorders - epidemiology | von Willebrand Diseases - diagnosis | Blood Platelet Disorders - diagnosis | Skin Diseases - etiology | Serotonin - metabolism | Coagulation Protein Disorders - diagnosis | Epinephrine - pharmacology | Hemoglobins - analysis
Journal Article
Nature, ISSN 0028-0836, 11/2014, Volume 515, Issue 7526, pp. 216 - 221
Journal Article
Journal Article
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