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Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes

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Cover of 'Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes'

Table of Contents

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    Book Overview
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    Chapter 1 Embryology of Neurocutaneous Syndromes
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    Chapter 2 Vascular Birthmarks of Infancy: Phace Association (Pascual-Castroviejo Type II Syndrome) and Cobb Syndrome
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    Chapter 3 Neurofibromatosis type 1 & Related Disorders
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    Chapter 4 Neurofibromatosis type 2 and related disorders
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    Chapter 5 The Tuberous Sclerosis Complex
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    Chapter 6 Von Hippel-Lindau Disease
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    Chapter 7 Klippel-Tranaunay, Parkes Weber and Sturge-Weber Syndromes (Including Kasabach-Merrit Phenomena)
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    Chapter 8 Klippel-Trenaunay Syndrome
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    Chapter 9 Parkes Weber Syndrome
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    Chapter 10 Sturge-Weber Syndrome
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    Chapter 11 Osler-Weber-Rendu syndrome (Hereditary Hemorrhagic Telangiectasia)
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    Chapter 12 Macrocephaly-Cutis Marmorata Telangiectatica Congenita (Macrocephaly-Capillary Malformation)
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    Chapter 13 Blue Rubber Bleb Nevus Syndrome (Brbns)
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    Chapter 14 Wyburn-Mason Syndrome
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    Chapter 15 Maffucci Syndrome
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    Chapter 16 Hypomelanosis of Ito and Related Disorders (Pigmentary Mosaicism)
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    Chapter 17 Phylloid Hypomelanosis
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    Chapter 18 Incontinentia Pigmenti
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    Chapter 19 Silver Hair Syndromes: Chediak-Higashi Syndrome (CHS) and Griscelli Syndromes (GS)
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    Chapter 20 Leopard Syndrome
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    Chapter 21 Nevus of OTA
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    Chapter 22 Phacomatosis Pigmentokeratotica
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    Chapter 23 Phakomatosis Pigmentovascularis
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    Chapter 24 Speckled Lentiginous Nevus Syndrome
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    Chapter 25 Cutis Tricolor (Ruggieri-Happle Syndrome)
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    Chapter 26 Neurocutaneous Melanosis
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    Chapter 27 Genetics of Pten Hamartoma Tumor Syndrome (PHTS)
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    Chapter 28 Lhermitte-Duclos and Cowden Disease Complex
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    Chapter 29 Bannayan-Riley-Ruvalcaba Syndrome
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    Chapter 30 Encephalocraniocutaneous Lipomatosis (Haberland Syndrome)
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    Chapter 31 Proteus Syndrome
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    Chapter 32 Epidermal Nevus Syndromes
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    Chapter 33 Schimmelpenning-Feuerstein-Mims Syndrome (Nevus Sebaceous Syndrome)
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    Chapter 34 Inflammatory Linear Verrucous Epidermal Nevus (Ilven)
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    Chapter 35 Nevus Comedonicus Syndrome
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    Chapter 36 Becker’s Nevus Syndrome (Pigmentary Hairy Epidermal Nevus)
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    Chapter 37 Child Syndrome
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    Chapter 38 Chondrodysplasia Punctata (Cdp) Conradi-Hunermann-Happle Type (Cdpx2)
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    Chapter 39 SjÖgren-Larsson Syndrome
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    Chapter 40 Kid Syndrome (Keratitis-Ichthyosis-Deafness)
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    Chapter 41 Papillon-Lefèvre Syndrome (PLS)
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    Chapter 42 Richner-Hanhart Syndrome (Tyrosine Transaminase Deficiency)
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    Chapter 43 Darier’s Disease
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    Chapter 44 Dyskeratosis Congenita
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    Chapter 45 Nevoid Basal Cell Carcinoma (Gorlin) Syndrome
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    Chapter 46 Multiple Endocrine Neoplasia Type 2B
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    Chapter 47 Turcot Syndrome
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    Chapter 48 Degos’ Disease (Malignant Atrophic Papulosis)
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    Chapter 49 Ataxia-Telangiectasia
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    Chapter 50 Nijmegen Breakage Syndrome
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    Chapter 51 Xeroderma Pigmentosum
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    Chapter 52 Cockayne Syndrome
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    Chapter 53 Trichothiodystrophy
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    Chapter 54 Progeria and Progeroid Syndromes (Premature Ageing Disorders)
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    Chapter 55 Focal Dermal Hypoplasia Syndrome (Goltz Syndrome)
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    Chapter 56 Ehlers-Danlos Syndromes
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    Chapter 57 Lipoid proteinosis
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    Chapter 58 Progressive facial hemiatrophy (parry-romberg syndrome)
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    Chapter 59 Linear scleroderma (morphoea) “en coup de sabre”
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    Chapter 60 Unilateral Somatic and Intracranial Hypoplasia
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    Chapter 61 Oculocerebrocutaneous Syndrome (Delleman Syndrome)
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    Chapter 62 Cerebello-Trigeminal Dermal Dysplasia (Gomez-Lopez-Hernandez Syndrome)
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    Chapter 63 Macrodactyly-Lipofibromatous Hamartoma of Nerves
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    Chapter 64 Chime Syndrome (Zunich Syndrome)
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    Chapter 65 Hypohidrotic Ectodermal Dysplasia (HED)
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    Chapter 66 Costello Syndrome and the Ras-Extracellular Signal Regulated Kinase (ERK) Pathway
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    Chapter 67 Anderson-Fabry Disease
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    Chapter 68 Cerebrotendinous Xanthomatosis
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    Chapter 69 Giant Axonal Neuropathy
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    Chapter 70 Lesch-Nyhan Syndrome
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    Chapter 71 The Skin as a Clue for the Diagnosis of Inherited Metabolic Disorders
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    Chapter 72 Skin Involvement as a Clinical Marker of Neuromuscular Disorders
Overall attention for this book and its chapters
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Citations

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Readers on

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Title
Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes
Published by
Springer Vienna, October 2009
DOI 10.1007/978-3-211-69500-5
ISBNs
978-3-21-121396-4, 978-3-21-169500-5
Editors

Ruggieri, Martino, Pascual-Castroviejo, Ignacio, Rocco, Concezio

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 17 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 17 100%

Demographic breakdown

Readers by professional status Count As %
Unspecified 3 18%
Student > Ph. D. Student 3 18%
Other 2 12%
Student > Master 2 12%
Student > Postgraduate 2 12%
Other 2 12%
Unknown 3 18%
Readers by discipline Count As %
Medicine and Dentistry 8 47%
Unspecified 3 18%
Agricultural and Biological Sciences 2 12%
Biochemistry, Genetics and Molecular Biology 1 6%
Unknown 3 18%