188 related articles for article (PubMed ID: 20543023)
21. Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutation.
Bessis D; Miquel J; Bourrat E; Chiaverini C; Morice-Picard F; Abadie C; Manna F; Baumann C; Best M; Blanchet P; Bursztejn AC; Capri Y; Coubes C; Giuliano F; Guillaumont S; Hadj-Rabia S; Jacquemont ML; Jeandel C; Lacombe D; Mallet S; Mazereeuw-Hautier J; Molinari N; Pallure V; Pernet C; Philip N; Pinson L; Sarda P; Sigaudy S; Vial Y; Willems M; Geneviève D; Verloes A; Cavé H
Br J Dermatol; 2019 Jun; 180(6):1438-1448. PubMed ID: 30417923
[TBL] [Abstract][Full Text] [Related]
22. Co-occurrence of hypertrophic cardiomyopathy and myeloproliferative disorder in a neonate with Noonan syndrome carrying Thr73Ile mutation in PTPN11.
Yagasaki H; Nakane T; Hasebe Y; Watanabe A; Kise H; Toda T; Koizumi K; Hoshiai M; Sugita K
Am J Med Genet A; 2015 Dec; 167A(12):3144-7. PubMed ID: 26286251
[TBL] [Abstract][Full Text] [Related]
23. Language and phonological skills in children at high risk of reading difficulties.
Carroll JM; Snowling MJ
J Child Psychol Psychiatry; 2004 Mar; 45(3):631-40. PubMed ID: 15055381
[TBL] [Abstract][Full Text] [Related]
24. Noonan syndrome: psychological and psychiatric aspects.
Verhoeven W; Wingbermühle E; Egger J; Van der Burgt I; Tuinier S
Am J Med Genet A; 2008 Jan; 146A(2):191-6. PubMed ID: 18080322
[TBL] [Abstract][Full Text] [Related]
25. Factors affecting articulation skills in children with velocardiofacial syndrome and children with cleft palate or velopharyngeal dysfunction: a preliminary report.
Baylis AL; Munson B; Moller KT
Cleft Palate Craniofac J; 2008 Mar; 45(2):193-207. PubMed ID: 18333642
[TBL] [Abstract][Full Text] [Related]
26. Phonological awareness, reading accuracy and spelling ability of children with inconsistent phonological disorder.
Holm A; Farrier F; Dodd B
Int J Lang Commun Disord; 2008; 43(3):300-22. PubMed ID: 17852519
[TBL] [Abstract][Full Text] [Related]
27. Intellectual development in Noonan syndrome: a longitudinal study.
Roelofs RL; Janssen N; Wingbermühle E; Kessels RP; Egger JI
Brain Behav; 2016 Jul; 6(7):e00479. PubMed ID: 27247851
[TBL] [Abstract][Full Text] [Related]
28. Reading and spelling abilities in children with severe speech impairments and cerebral palsy at 6, 9, and 12 years of age in relation to cognitive development: a longitudinal study.
Dahlgren Sandberg A
Dev Med Child Neurol; 2006 Aug; 48(8):629-34. PubMed ID: 16836773
[TBL] [Abstract][Full Text] [Related]
29. Duplication of chromosome band 12q24.11q24.23 results in apparent Noonan syndrome.
Shchelochkov OA; Patel A; Weissenberger GM; Chinault AC; Wiszniewska J; Fernandes PH; Eng C; Kukolich MK; Sutton VR
Am J Med Genet A; 2008 Apr; 146A(8):1042-8. PubMed ID: 18348260
[TBL] [Abstract][Full Text] [Related]
30. Two cases of Noonan syndrome with severe respiratory and gastroenteral involvement and the SOS1 mutation F623I.
Fabretto A; Kutsche K; Harmsen MB; Demarini S; Gasparini P; Fertz MC; Zenker M
Eur J Med Genet; 2010; 53(5):322-4. PubMed ID: 20673819
[TBL] [Abstract][Full Text] [Related]
31. Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations.
Athota JP; Bhat M; Nampoothiri S; Gowrishankar K; Narayanachar SG; Puttamallesh V; Farooque MO; Shetty S
BMC Med Genet; 2020 Mar; 21(1):50. PubMed ID: 32164556
[TBL] [Abstract][Full Text] [Related]
32. PTPN11 mutations are associated with mild growth hormone resistance in individuals with Noonan syndrome.
Binder G; Neuer K; Ranke MB; Wittekindt NE
J Clin Endocrinol Metab; 2005 Sep; 90(9):5377-81. PubMed ID: 15985475
[TBL] [Abstract][Full Text] [Related]
33. Co-occurring SHOC2 and PTPN11 mutations in a patient with severe/complex Noonan syndrome-like phenotype.
Ekvall S; Hagenäs L; Allanson J; Annerén G; Bondeson ML
Am J Med Genet A; 2011 Jun; 155A(6):1217-24. PubMed ID: 21548061
[TBL] [Abstract][Full Text] [Related]
34. Early preschool processing abilities predict subsequent reading outcomes in bilingual Spanish-Catalan children with Specific Language Impairment (SLI).
Aguilar-Mediavilla E; Buil-Legaz L; Pérez-Castelló JA; Rigo-Carratalà E; Adrover-Roig D
J Commun Disord; 2014; 50():19-35. PubMed ID: 24767985
[TBL] [Abstract][Full Text] [Related]
35. [Phenotype variability in Noonan syndrome patients with and without PTPN11 mutation].
Ferreira LV; Souza SA; Montenegro LR; Arnhold IJ; Pasqualini T; Heinrich JJ; Keselman AC; Mendonça BB; Jorge AA
Arq Bras Endocrinol Metabol; 2007 Apr; 51(3):450-6. PubMed ID: 17546245
[TBL] [Abstract][Full Text] [Related]
36. Noonan syndrome: Severe phenotype and PTPN11 mutations.
Carrasco Salas P; Gómez-Molina G; Carreto-Alba P; Granell-Escobar R; Vázquez-Rico I; León-Justel A
Med Clin (Barc); 2019 Jan; 152(2):62-64. PubMed ID: 29703613
[TBL] [Abstract][Full Text] [Related]
37. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity.
Tartaglia M; Kalidas K; Shaw A; Song X; Musat DL; van der Burgt I; Brunner HG; Bertola DR; Crosby A; Ion A; Kucherlapati RS; Jeffery S; Patton MA; Gelb BD
Am J Hum Genet; 2002 Jun; 70(6):1555-63. PubMed ID: 11992261
[TBL] [Abstract][Full Text] [Related]
38. Speech, language, and cognition in preschool children with epilepsy.
Selassie GR; Viggedal G; Olsson I; Jennische M
Dev Med Child Neurol; 2008 Jun; 50(6):432-8. PubMed ID: 18422681
[TBL] [Abstract][Full Text] [Related]
39. Children's history of speech-language difficulties: genetic influences and associations with reading-related measures.
DeThorne LS; Hart SA; Petrill SA; Deater-Deckard K; Thompson LA; Schatschneider C; Davison MD
J Speech Lang Hear Res; 2006 Dec; 49(6):1280-93. PubMed ID: 17197496
[TBL] [Abstract][Full Text] [Related]
40. Acute lymphoblastic leukemia in the context of RASopathies.
Cavé H; Caye A; Strullu M; Aladjidi N; Vignal C; Ferster A; Méchinaud F; Domenech C; Pierri F; Contet A; Cacheux V; Irving J; Kratz C; Clavel J; Verloes A
Eur J Med Genet; 2016 Mar; 59(3):173-8. PubMed ID: 26855057
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]