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in neurofibromatosis. This book represents a reference source for researchers, healthcare professionals from various fields, as well as students, about;
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Neurofibromatosis type 1 (NF1) is a common disease affecting 1 in 4000 individuals world-wide. Symptoms include facial and body;
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A great deal is now known about neurofibromatosis type 1, particularly as a result of the identification of its causative gene by;
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Neurofibromatosis Type 1 (NF1) is a hereditary neurocutaneous tumour disorder that owes many of its most common features to abnormalities;
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This monograph includes five chapters about neurofibromatosis type 1 (NF1), a condition characterised by changes in skin colouring and the;
Vergelijkbare producten zoals Neurofibromatosis Type 1
Neurofibromatosis Type 1 (NF1) is a relatively common genetic disorder that predisposes affected individuals for developing multiple;
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, ovary, prostate and melanoma, and separate chapters cover cancer predisposing syndromes such as neurofibromatosis, familial adenomatous;
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> 5 new long cases, including hypopituitarism, neurofibromatosis type 1 and Rett syndrome 8 new short cases,
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earmarked appropriations for programs of biomedical research on prostate, breast, and ovarian cancer; neurofibromatosis; tuberous sclerosis; and;
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acquired lesions. Subsequent chapters cover generalized orthopedic diseases such as neurofibromatosis and osteogenesis imperfecta, infectious;
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neurofibromatosis type 1; avidity of autoantibodies against antigens in nervous tissue; epidemiological study of childhood epilepsy using the newly;
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; Neurofibromatosis and Related Disorders; Marfan, Loeys Dietz, and Other Syndromes Causing Arterial Fragility; Ehlers Danlos Syndromes and Related Disorders;
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A description of the social, educational, and economic impact of living with a neurological genetic disorder, neurofibromatosis 1. The many;
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, Intraoperative and Postoperative - Facial nerve; Neurofibromatosis Type 2 and Genetics; The Art of Management Decision Making: From Intuition to Evidence;
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neurofibromatosis. Reviews current information on congenital, inflammatory, infectious, neoplastic, traumatic conditions of the orbit and accessory;
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answers to what she feared the most. Her nightmare turned into reality, and Zachary was diagnosed with neurofibromatosis. When the disorder;
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Neurofibromatosis Type II and other skullbase disorders, and Biologics in treatment of autoimmune ear disorders. ;
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, neuromuscular, tumors, neurofibromatosis, and more. All too often in other works, too much attention has been focused on how to put in metalwork;
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syndromes include, neurofibromatosis, Sturge-Weber syndrome, tuberous sclerosis, ataxia-telangiectasia, and von Hippel-Lindau disease. Symptoms vary;
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of neuro-oncology: primary CNS tumors, brain and leptomeningeal metastases, inherited tumor syndromes of the nervous system (e.g. neurofibromatosis;
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neurofibromatosis and other genetic syndromes. It then discusses tumors at special sites, from brainstem tumors to peripheral nerve tumors, tumors of the;
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neurofibromatosis (NF1 and NF2), tuberous sclerosis (TSC1 and TSC2), and myotonic dystrophy. X-linked disorders producing mental retardation in syndromal;
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manifestation of internal malignancy, neurofibromatosis, tuberous sclerosis, photoaging, photosensivity, laser treatment for skin-tightening, toxins and;
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options for patients with neurofibromatosis type 2 In-depth information on key aspects of patient care, such as patient selection, preoperative;
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neurofibromatosis, informed by the latest developments in molecular biology and histologic imaging. See current dermatologic concepts;
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modalities for sporadic and neurofibromatosis type 2-associated vestibular schwannoma. Key Features Evaluation, surgical and nonsurgical;
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