Literature DB >> 3543368

Noonan syndrome.

J E Allanson.   

Abstract

Entities:  

Mesh：

Year:  1987        PMID： 3543368      PMCID： PMC1049850          DOI： 10.1136/jmg.24.1.9

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  36 in total

1.  Malignant hyperthermia associated with myopathy and normal muscle enzymes.

Authors:  A M Kaplan; P S Bergeson; S A Gregg; R G Curless
Journal:  J Pediatr       Date:  1977-09       Impact factor: 4.406

2.  The orthopedic aspects of the fetal alcohol syndrome.

Authors:  P G Spiegel; W M Pekman; B H Rich; C N Versteeg; V Nelson; M Dudnikov
Journal:  Clin Orthop Relat Res       Date:  1979 Mar-Apr       Impact factor: 4.176

3.  Growth and pubertal development in five boys with Noonan's syndrome.

Authors:  G Theintz; M O Savage
Journal:  Arch Dis Child       Date:  1982-01       Impact factor: 3.791

4.  Noonan phenotype with polydactyly.

Authors:  A Grix; B D Hall
Journal:  Birth Defects Orig Artic Ser       Date:  1979

5.  Postoperative hyperpyrexia in a case of Noonan's syndrome.

Authors:  H S Rissam; S R Mittal; P L Wahi; P S Bidwai
Journal:  Indian Heart J       Date:  1982 May-Jun

6.  Chiari (type 1) malformation and syringomyelia in a patient with Noonan's syndrome.

Authors:  A Peiris; M J Ball
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-08       Impact factor: 10.154

7.  Ullrich-Turner syndrome in the male: review of the literature and report of a case with lymphocytic (Hashimoto's) thyroiditis.

Authors:  E Chaves-Carballo; A B Hayles
Journal:  Mayo Clin Proc       Date:  1966-12       Impact factor: 7.616

8.  Keratosis pilaris atrophicans faciei (ulerythema ophryogenes): a cutaneous marker in the Noonan syndrome.

Authors:  D O Pierini; A M Pierini
Journal:  Br J Dermatol       Date:  1979-04       Impact factor: 9.302

9.  Familial Williams syndrome.

Authors:  X Cortada; K Taysi; A F Hartmann
Journal:  Clin Genet       Date:  1980-09       Impact factor: 4.438

10.  Noonan's syndrome. IQ and specific disabilities.

Authors:  J Money; M E Kalus
Journal:  Am J Dis Child       Date:  1979-08
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  87 in total

1.  Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.

Authors:  M Sharland; R Taylor; M A Patton; S Jeffery
Journal:  J Med Genet       Date:  1992-03       Impact factor: 6.318

2.  A clinical study of Noonan syndrome.

Authors:  M Sharland; M Burch; W M McKenna; M A Paton
Journal:  Arch Dis Child       Date:  1992-02       Impact factor: 3.791

Review 3.  Ras and Rap signaling in synaptic plasticity and mental disorders.

Authors:  Ruth L Stornetta; J Julius Zhu
Journal:  Neuroscientist       Date:  2010-04-29       Impact factor: 7.519

4.  Genome-wide linkage analysis for ocular and nasal anthropometric traits in a Mongolian population.

Authors:  Sun-Wha Im; Hyun-Jin Kim; Mi Kyeong Lee; Jae-hyuk Yi; Ganchimeg Jargal; Joohon Sung; Sung-il Cho; Jong-Il Kim
Journal:  Exp Mol Med       Date:  2010-12-31       Impact factor: 8.718

5.  Noonan syndrome mutation Q79R in Shp2 increases proliferation of valve primordia mesenchymal cells via extracellular signal-regulated kinase 1/2 signaling.

Authors:  Maike Krenz; Katherine E Yutzey; Jeffrey Robbins
Journal:  Circ Res       Date:  2005-09-15       Impact factor: 17.367

6.  PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome.

Authors:  Jung Min Ko; Jae-Min Kim; Gu-Hwan Kim; Han-Wook Yoo
Journal:  J Hum Genet       Date:  2008-11-20       Impact factor: 3.172

7.  Altered lymphatics in an ovine model of congenital heart disease with increased pulmonary blood flow.

Authors:  Sanjeev A Datar; Eric G Johnson; Peter E Oishi; Michael Johengen; Eric Tang; Angela Aramburo; Jubilee Barton; Hsuan-Chang Kuo; Stephen Bennett; Konstantine Xoinis; Bhupinder Reel; Gokhan Kalkan; Eniko Sajti; Oscar Osorio; Gary W Raff; Michael A Matthay; Jeffrey R Fineman
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2011-12-29       Impact factor: 5.464

8.  Noonan syndrome.

Authors:  A E Lin
Journal:  J Med Genet       Date:  1988-01       Impact factor: 6.318

9.  Noonan's and DiGeorge syndromes with monosomy 22q11.

Authors:  D I Wilson; S B Britton; C McKeown; D Kelly; I E Cross; S Strobel; P J Scambler
Journal:  Arch Dis Child       Date:  1993-02       Impact factor: 3.791

10.  Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair.

Authors:  Viviana Cordeddu; Elia Di Schiavi; Len A Pennacchio; Avi Ma'ayan; Anna Sarkozy; Valentina Fodale; Serena Cecchetti; Alessio Cardinale; Joel Martin; Wendy Schackwitz; Anna Lipzen; Giuseppe Zampino; Laura Mazzanti; Maria C Digilio; Simone Martinelli; Elisabetta Flex; Francesca Lepri; Deborah Bartholdi; Kerstin Kutsche; Giovanni B Ferrero; Cecilia Anichini; Angelo Selicorni; Cesare Rossi; Romano Tenconi; Martin Zenker; Daniela Merlo; Bruno Dallapiccola; Ravi Iyengar; Paolo Bazzicalupo; Bruce D Gelb; Marco Tartaglia
Journal:  Nat Genet       Date:  2009-08-16       Impact factor: 38.330
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