Multidisciplinary Approach To Neurofibromatosis Type 1
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Author |
: Gianluca Tadini |
Publisher |
: Springer Nature |
Total Pages |
: 316 |
Release |
: 2020-06-02 |
ISBN-10 |
: 9783319924502 |
ISBN-13 |
: 3319924508 |
Rating |
: 4/5 (02 Downloads) |
Synopsis Multidisciplinary Approach to Neurofibromatosis Type 1 by : Gianluca Tadini
This volume offers an update of the clinical signs, diagnostic criteria (including molecular diagnosis) and targeted therapies for a particular type of genodermatosis, providing a handy and unique tool for early diagnosis. In recent years, our understanding of genodermatosis and neurocutaneous syndromes has increased, but although Type 1 Neurofibromatosis (NF1) is the most common neuroectodermal disorder and involves a large number of patients and medical disciplines, this syndrome remains underestimated, often misdiagnosed thus leading to inaccurate treatment. The literature on the molecular and pathogenetic aspects is ample, but current clinical approaches, classification, diagnostic criteria and treatment protocols are outdated, creating difficulties in early diagnosis and treatment. As such, a chapter is devoted renewing current diagnostic criteria; it includes clinical and molecular data, to offer a sound, updated discussion basis for a consensus conference. NF1 is a “time-dependent” disorder, meaning that the onset of clinical signs are closely linked to patient age and the book discusses this particularly neglected aspect extensively, as well as the latest molecular diagnosis techniques, which are highly sensitive have not been included in the diagnostic criteria. It also explains the role of the RAS-MAPK pathway and genotype-phenotype correlations. In addition it explores new concepts concerning the pathogenesis of neurofibromas and other hamarthomas and their relevance for a modern therapeutical approach with targeted molecular drugs, as well as newly discovered aspects of NF1 in all internal organs, together with their diagnostic counterparts. A chapter on mosaic neurofibromatosis is also included. There is a particular focus on differential diagnosis (i.e. other diseases with café-au-lait macules), and the recently described Legius syndrome will be presented directly by Prof Eric Legius. All chapters are easy-to-understand, up-to-date, comprehensive and concise tools and are intended for a wide range of professionals involved with genetic disorders of the skin and neurocutaneous diseases: dermatologists, pediatricians, neurologists, oncologists and general practitioners.
Author |
: Paolo Curatolo |
Publisher |
: John Libbey Eurotext |
Total Pages |
: 247 |
Release |
: 2006 |
ISBN-10 |
: 9782742006090 |
ISBN-13 |
: 2742006095 |
Rating |
: 4/5 (90 Downloads) |
Synopsis Neurocutaneous Syndromes in Children by : Paolo Curatolo
Neurocutaneous Syndromes unify a group of rare neurological disorders in which the initial identification depends on simple visual disgnosis. They include a large group of neurological disorders which feature cutaneous and ocular lesions, brain malformations, central and peripheral brain tumours, mental retardation, seizures and psychiatric problems. In the last few years, our knowledge of neurocutaneous syndromes has increased substantially. The aim of this volume is to provide an updated developmental perspective on these multifaceted conditions and to review their major clinical features, in particular their embryological basis, clinical molecular genetics, diagnostic protocols and novel therapeutic approaches.
Author |
: Meena Upadhyaya |
Publisher |
: Springer Science & Business Media |
Total Pages |
: 711 |
Release |
: 2013-01-29 |
ISBN-10 |
: 9783642328640 |
ISBN-13 |
: 3642328644 |
Rating |
: 4/5 (40 Downloads) |
Synopsis Neurofibromatosis Type 1 by : Meena Upadhyaya
Neurofibromatosis type 1 (NF1), caused by mutational inactivation of the NF1 tumour suppressor gene, is one of the most common dominantly inherited human disorders, affecting 1 in 3000 individuals worldwide. This book presents in concise fashion, but as comprehensively as possible, our current state of knowledge on the molecular genetics, molecular biology and cellular biology of this tumour predisposition syndrome. Written by internationally recognized experts in the field, the 44 chapters that constitute this edited volume provide the reader with a broad overview of the clinical features of the disease, the structure and expression of the NF1 gene, its germ line and somatic mutational spectra and genotype-phenotype relationships, the structure and function of its protein product (neurofibromin), NF1 modifying loci, the molecular pathology of NF1-associated tumours, animal models of the disease, psycho-social aspects and future prospects for therapeutic treatment.
Author |
: Concezio Di Rocco |
Publisher |
: Springer |
Total Pages |
: 0 |
Release |
: 2020-07-14 |
ISBN-10 |
: 3319721674 |
ISBN-13 |
: 9783319721675 |
Rating |
: 4/5 (74 Downloads) |
Synopsis Textbook of Pediatric Neurosurgery by : Concezio Di Rocco
This book documents the state of the art in pediatric neurosurgery with the intention of providing a comprehensive guide to the management of the full range of pediatric neurosurgical disorders that will aid in the delivery of optimal care. Detailed practical instruction, taking into account recent advances, is provided on the neurosurgical treatment of congenital brain malformations, cerebrovascular diseases, head injuries and spinal trauma, infections, functional disorders, congenital and developmental spinal disorders, and brain and spinal tumors. Pearls and pitfalls are highlighted, and attention drawn to the most useful tips and tricks. Information is also included on relevant related topics, including the principles of neuroimaging, the physiological responses of newborns, infants, and children to neurosurgical trauma, preoperative evaluation, anesthesiology and intensive care, and other forms of therapy. The authors are renowned experts in the field, and the text is supported by a wealth of high-quality images. Handbook of Pediatric Neurosurgery will be of value for neurosurgeons of all levels of experience, as well as for pediatricians, neuroradiologists, neuropathologists, and neuro-oncologists.
Author |
: Supriya Mallick |
Publisher |
: Springer Nature |
Total Pages |
: 423 |
Release |
: 2021-07-24 |
ISBN-10 |
: 9789811626593 |
ISBN-13 |
: 9811626596 |
Rating |
: 4/5 (93 Downloads) |
Synopsis Evidence based practice in Neuro-oncology by : Supriya Mallick
This book provides evidence-based management in neuro-oncology covering all aspects such as pathology, radiology, surgery, radiation, and chemotherapy.The field of neuro-oncology is rapidly evolving and new evidence is coming out every day towards the optimal management of brain tumors. This necessitates a requirement of a complete guide that shall provide an evidence-based and personalized approach towards dealing with patients. This book also covers recent advances in personalized treatment formed through the relevant basis of anatomy, imaging, radiology, surgical, radiation and systemic treatment of brain and spinal tumors. In addition it also covers the , practical aspects of the planning of the Gamma knife and other radio surgical aspects. The book shall provide valuable assistance to practicing neuro-oncologists to practice better evidence-based personalized medicine.
Author |
: Ruggero Caputo |
Publisher |
: CRC Press |
Total Pages |
: 448 |
Release |
: 2005-12-12 |
ISBN-10 |
: 9781841842516 |
ISBN-13 |
: 1841842516 |
Rating |
: 4/5 (16 Downloads) |
Synopsis Atlas of Genodermatoses by : Ruggero Caputo
A lavishly illustrated guide to almost 200 inherited diseases of the skin, hair, and nails. Each entry includes synonyms, age of onset, clinical findings, complications, course, laboratory findings, diagnosis, therapy, and key references, adding up to far more than just a collection of photographs. In addition to being a clinical primer, this is also a work of scientific research and contains the first printed description of two new syndromes. The fast-moving world of genetic research means that the latest genetic correlations, included here, render previous texts out of date. All specialists in Dermatology and Pediatrics should find this an invaluable front-line resource in the clinic.
Author |
: Peter Igaz |
Publisher |
: Springer Nature |
Total Pages |
: 476 |
Release |
: 2019-10-06 |
ISBN-10 |
: 9783030259051 |
ISBN-13 |
: 3030259056 |
Rating |
: 4/5 (51 Downloads) |
Synopsis Genetics of Endocrine Diseases and Syndromes by : Peter Igaz
This book provides a comprehensive overview of the genetic basis underlying endocrine diseases. It covers both the molecular and clinical consequences of these genetic defects, as well as the relevance for clinical care, highlighting issues of genetic counseling. Several endocrine diseases have a genetic background, and contemporary research in the field plays a crucial role in the clinical care of endocrine diseases. In recent years, there have been major developments in our understanding of the genetic basis of endocrine diseases. Several novel genes and mutations predisposing individuals to monogenic endocrine diseases have been discovered, and with the advent of next generation sequencing, a huge amount of new data has become available. Further, novel molecular mechanisms, such as genomic imprinting, have been implicated in the pathogenesis of endocrine diseases. A better understanding of the genetic background of these diseases is relevant not only from the research perspective, but also in terms of clinical care. As such, this book is an essential read for both researchers and clinicians working in the field.
Author |
: World Health Organization |
Publisher |
: World Health Organization |
Total Pages |
: 24 |
Release |
: 2006 |
ISBN-10 |
: 9789241593618 |
ISBN-13 |
: 924159361X |
Rating |
: 4/5 (18 Downloads) |
Synopsis Primary Ear and Hearing Care Training Resource by : World Health Organization
Although half of all deafness and hearing impairment is avoidable, an estimated 278 million people worldwide are living with disabling hearing impairment (moderate or worse level of hearing loss in the better hearing ear). Many more have mild hearing loss and/or ear diseases. One quarter of hearing impairment begins during childhood, and 80% of all deaf and hearing impaired people live in low and middle income countries. These problems can be life-long and sometimes life-threatening; they may have profound effects on: inter-personal communication, education, employment prospects, social relationships and through stigmatization. They produce substantial economic burdens on countries. Some of the most effective and cost-effective interventions against ear and hearing problems can be implemented at the primary level by trained primary ear and hearing care (PEHC) workers or primary health care (PHC) workers or their equivalents. Used on a large scale, these interventions will have a major impact on the burden of ear disease and hearing loss. However most developing countries do not have PEHC workers and the topic is hardly addressed in the training of PHC workers. The Primary Ear and Hearing Care Training Resource manuals provide practical information and guidance and can be used as part of a training course, stand-alone training module or in a self-taught manner. They are designed to be useful to a wide range of primary health care personnel. The manuals can also be used to help communities understand common causes of deafness and hearing impairment and ways to prevent and/or treat the conditions.
Author |
: Angela C. Hirbe |
Publisher |
: MDPI |
Total Pages |
: 172 |
Release |
: 2020-11-18 |
ISBN-10 |
: 9783039434893 |
ISBN-13 |
: 3039434896 |
Rating |
: 4/5 (93 Downloads) |
Synopsis Genomics and Models of Nerve Sheath Tumors by : Angela C. Hirbe
Nerve sheath tumors can be a significant cause of morbidity for many patients. These include benign tumors such as schwannomas, diffuse and plexiform neurofibromas, and atypical neurofibromas, as well as the aggressive soft tissue sarcoma known as the malignant peripheral nerve sheath tumor (MPNST). Nerve sheath tumors occur sporadically and in the context of the clinical neuro-genetic tumor predisposition syndromes neurofibromatosis type 1 (NF1) and type 2 (NF2). Historically, the mainstay of treatment for nerve sheath tumors has been surgery. However, for both benign and malignant nerve sheath tumors, there is a high recurrence rate, highlighting the pressing need for novel therapies. As we have entered the genomic era, the hope is that an improved understanding of the genetics, and therefore the biology, of these tumors will ultimately lead to therapies that result in better outcomes. In this Special Issue, we include both review articles and original research related to the genomic understanding and modeling of schwannomas, plexiform and diffuse neurofibromas, atypical neurofibromas, and malignant peripheral nerve sheath tumors as well as genomic methods being developed and applied to advance our understanding of these tumors.
Author |
: Gregory O'Brien |
Publisher |
: Cambridge University Press |
Total Pages |
: 236 |
Release |
: 1995 |
ISBN-10 |
: 1898683069 |
ISBN-13 |
: 9781898683063 |
Rating |
: 4/5 (69 Downloads) |
Synopsis Behavioural Phenotypes by : Gregory O'Brien
A timely distillation of current thinking on the presentation of behavioural disorders and their origins.