Literature DB >> 3103548

Noonan's syndrome and neurofibromatosis.

A Shuper, M Mukamel, M Mimouni, R Steinherz.   

Abstract

A child with Noonan syndrome and multiple cafe au lait spots, compatible in size and number with von Recklinghausen's neurofibromatosis, is presented. These features may represent a distinct genetic entity rather than the coincidence of two diseases.

Entities:  

Mesh：

Year:  1987        PMID： 3103548      PMCID： PMC1778243          DOI： 10.1136/adc.62.2.196

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


  5 in total

1.  Noonan phenotype associated with neurofibromatosis.

Authors:  J E Allanson; J G Hall; M I Van Allen
Journal:  Am J Med Genet       Date:  1985-07

2.  The neurofibromatosis-Noonan syndrome.

Authors:  J M Opitz; D D Weaver
Journal:  Am J Med Genet       Date:  1985-07

3.  The neurofibromatosis-Noonan syndrome.

Authors:  H M Mendez
Journal:  Am J Med Genet       Date:  1985-07

Review 4.  Noonan syndrome: a review.

Authors:  H M Mendez; J M Opitz
Journal:  Am J Med Genet       Date:  1985-07

Review 5.  Von Recklinghausen neurofibromatosis.

Authors:  V M Riccardi
Journal:  N Engl J Med       Date:  1981-12-31       Impact factor: 91.245
  5 in total
  3 in total

1.  Noonan's syndrome and neurofibromatosis.

Authors:  T P Mann
Journal:  Arch Dis Child       Date:  1988-02       Impact factor: 3.791

2.  NF1 gene mutations represent the major molecular event underlying neurofibromatosis-Noonan syndrome.

Authors:  Alessandro De Luca; Irene Bottillo; Anna Sarkozy; Claudio Carta; Cinzia Neri; Emanuele Bellacchio; Annalisa Schirinzi; Emanuela Conti; Giuseppe Zampino; Agatino Battaglia; Silvia Majore; Maria M Rinaldi; Massimo Carella; Bruno Marino; Antonio Pizzuti; Maria Cristina Digilio; Marco Tartaglia; Bruno Dallapiccola
Journal:  Am J Hum Genet       Date:  2005-10-26       Impact factor: 11.025

3.  Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome.

Authors:  Doğuş Vurallı; Nazlı Gönç; Dominique Vidaud; Alev Özön; Ayfer Alikaşifoğlu; Nurgün Kandemir
Journal:  J Clin Res Pediatr Endocrinol       Date:  2015-12-18
  3 in total

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