Clinical aspects of neurofibromatosis 1. (Q33869028)

29 July 2017

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title

Clinical aspects of neurofibromatosis 1. (English)

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29 July 2017

North KN

1

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29 July 2017

publication date

1 January 1998

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European Journal of Paediatric Neurology

29 July 2017

published in

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29 July 2017

volume

2

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29 July 2017

issue

5

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29 July 2017

page(s)

223-231

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Von Recklinghausen neurofibromatosis. A clinical and population study in south-east Wales.

29 July 2017

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Neurofibromatosis type 1: review of the first 200 patients in an Australian clinic

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Relationship between café-au-lait spots as the only symptom and peripheral neurofibromatosis (NF1): a follow-up study

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Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage

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Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spots

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Familial café au lait spots: a variant of neurofibromatosis type 1.

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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor

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Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

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Type 1 neurofibromatosis and the pediatric patient

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Lisch nodules in neurofibromatosis type 1.

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Specific learning disability in children with neurofibromatosis type 1: significance of MRI abnormalities

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Neuropsychological profile of children with neurofibromatosis, brain tumor, or both.

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Intellectual impairment in neurofibromatosis 1.

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Cognitive function and academic performance in neurofibromatosis. 1: consensus statement from the NF1 Cognitive Disorders Task Force

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Precocious puberty in children with neurofibromatosis type 1.

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Natural history of optic pathway tumors in children with neurofibromatosis type 1: a longitudinal study.

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Evolution of white matter lesions in neurofibromatosis type 1: MR findings

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Neurofibromatosis type 1: pathologic substrate of high-signal-intensity foci in the brain

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Neurofibromatosis type 1: the cognitive phenotype.

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Neuropsychological significance of areas of high signal intensity on brain MRIs of children with neurofibromatosis

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Neurofibromatosis type 1 in childhood: correlation of MRI findings with intelligence

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Neurofibromatosis Type 1 Due to Germ-Line Mosaicism in a Clinically Normal Father

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Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

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7 January 2021

A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations

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The neurofibromatosis type 1 gene encodes a protein related to GAP

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7 January 2021

Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis

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7 January 2021

Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders

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7 January 2021

Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene

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7 January 2021

Distribution of 13 truncating mutations in the neurofibromatosis 1 gene

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7 January 2021

10.1016/S1090-3798(98)80035-4

Identifiers

DOI

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29 July 2017

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