Titlebook: Neurocutaneous Disorders; Phakomatoses & Hamar Martino Ruggieri,Ignacio Pascual-Castroviejo,Conce Book 2008 Springer-Verlag Vienna 2008 Hyp

胃口

書目名稱Neurocutaneous Disorders影響因子(影響力)




書目名稱Neurocutaneous Disorders影響因子(影響力)學科排名




書目名稱Neurocutaneous Disorders網(wǎng)絡公開度




書目名稱Neurocutaneous Disorders網(wǎng)絡公開度學科排名




書目名稱Neurocutaneous Disorders被引頻次




書目名稱Neurocutaneous Disorders被引頻次學科排名




書目名稱Neurocutaneous Disorders年度引用




書目名稱Neurocutaneous Disorders年度引用學科排名




書目名稱Neurocutaneous Disorders讀者反饋




書目名稱Neurocutaneous Disorders讀者反饋學科排名

蜿蜒而流

Von Hippel-Lindau Disease,lar, brainstem and spinal hemangioblastomas, and endolymphatic sac tumors (ELSTs). Visceral lesions include renal cell carcinomas (RCC), renal cysts, pheochromocytomas, pancreatic cysts and neuroendocrine tumors, as well as cystadenomas of the epididymis and broad ligament (Fig. 1).

legitimate

Osler-Weber-Rendu syndrome (Hereditary Hemorrhagic Telangiectasia),common than previously thought, and its association to brain, liver and pulmonary lesions are sources of substantial morbidity and mortality and represent even these days a continuing challenge for many sub-specialities (.).

Narcissist

Incontinentia Pigmenti,ted to non progressive, chronic central nervous system (CNS) involvement (.). Other anatomical regions are less frequently affected. Development of benign subungual tumors involving distal phalanges in adult age is not rare.

嫌惡

未開化

委屈

Maffucci Syndrome,s the World Health Organisation classifies the Maffucci syndrome as a subclass of enchondromatosis and defines it as a developmental disorder characterized by the presence of multiple cartilaginous masses and the presence of cutaneous, soft tissue or visceral haemangiomas (.).

ABIDE

Sturge-Weber Syndrome,features of this triad exist (.). Other clinical features associated with SWS are seizures, glaucoma, headache, transient stroke-like neurological deficits, and behavioural problems. Hemiparesis, hemiatrophy, and hemianopia may occur contralaterally to the cortical abnormality (.).

一回合

Embryology of Neurocutaneous Syndromes,tures that share in common developmental lesions of the skin and of the central and peripheral nervous systems. Subcutaneous and systemic involvement is common. In many of these conditions another feature is a tendency to develop tumors in multiple sites of the body. Many of these disorders are hama

CALL

Neurofibromatosis type 1 & Related Disorders, clinical diagnostic criteria and management guidelines have been developed (.; .; .; .; ., .; .; .; .; .). The genes for the two major forms, neurofibromatosis type 1 (NF1) and type 2 (NF2), have been cloned and the gene products, . and . (also called ., respectively, fully characterised (reviewed