92 related articles for article (PubMed ID: 27753652)
41. Noonan syndrome: prenatal diagnosis in a woman carrying a PTPN11 gene mutation.
González-Huerta NC; Valdés-Miranda JM; Pérez-Cabrera A; Pacheco-Cuellar G; González-Huerta LM; Cuevas-Covarrubias SA
J Matern Fetal Neonatal Med; 2010 Jul; 23(7):688-91. PubMed ID: 20064076
[TBL] [Abstract][Full Text] [Related]
42. Mutation analysis of the genes involved in the Ras-mitogen-activated protein kinase (MAPK) pathway in Korean patients with Noonan syndrome.
Lee ST; Ki CS; Lee HJ
Clin Genet; 2007 Aug; 72(2):150-5. PubMed ID: 17661820
[TBL] [Abstract][Full Text] [Related]
43. Neurofibromatosis-Noonan Syndrome: A Possible Paradigm of the Combination of Genetic and Epigenetic Factors.
Yapijakis C; Pachis N; Voumvourakis C
Adv Exp Med Biol; 2017; 987():151-159. PubMed ID: 28971455
[TBL] [Abstract][Full Text] [Related]
44. Interhemispheric subdural hematoma: an uncommon sequel of trauma.
Shankar A; Joseph M; Chandy MJ
Neurol India; 2003 Mar; 51(1):63-4. PubMed ID: 12865519
[TBL] [Abstract][Full Text] [Related]
45. Comprehensive genetic analysis of overlapping syndromes of RAS/RAF/MEK/ERK pathway.
Tumurkhuu M; Saitoh M; Sato A; Takahashi K; Mimaki M; Takita J; Takeshita K; Hama T; Oka A; Mizuguchi M
Pediatr Int; 2010 Aug; 52(4):557-62. PubMed ID: 20030748
[TBL] [Abstract][Full Text] [Related]
46. Copy number variants and rasopathies: germline KRAS duplication in a patient with syndrome including pigmentation abnormalities.
Gilbert-Dussardier B; Briand-Suleau A; Laurendeau I; Bilan F; Cavé H; Verloes A; Vidaud M; Vidaud D; Pasmant E
Orphanet J Rare Dis; 2016 Jul; 11(1):101. PubMed ID: 27450488
[TBL] [Abstract][Full Text] [Related]
47. Bilateral giant coronary aneurysms in a 40-year-old male with Noonan syndrome caused by a KRAS germline mutation.
Fujimoto N; Nakajima H; Sugiura E; Dohi K; Kanemitsu S; Yamada N; Aoki Y; Nakatani K; Shimpo H; Nobori T; Ito M
Int J Cardiol; 2014 May; 173(3):e63-6. PubMed ID: 24703799
[No Abstract] [Full Text] [Related]
48. [Familial Noonan syndrome].
Krüger G; Schumacher K; Mix M; Pelz L
Kinderarztl Prax; 1989 May; 57(5):245-8. PubMed ID: 2747123
[TBL] [Abstract][Full Text] [Related]
49. RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis.
Wong S; Tan YX; Loh AYT; Tan KY; Lee H; Aziz Z; Nelson SF; Özkan E; Kayserili H; Escande-Beillard N; Reversade B
EMBO Mol Med; 2023 May; 15(5):e17078. PubMed ID: 37066513
[TBL] [Abstract][Full Text] [Related]
50. Skull defects, alopecia, hypertelorism, and notched alae nasi caused by homozygous ALX4 gene mutation.
Kariminejad A; Bozorgmehr B; Alizadeh H; Ghaderi-Sohi S; Toksoy G; Uyguner ZO; Kayserili H
Am J Med Genet A; 2014 May; 164A(5):1322-7. PubMed ID: 24668755
[No Abstract] [Full Text] [Related]
51. Neonatal Noonan syndrome with a molluscoid cutaneous excess over the scalp.
Lacombe D; Taieb A; Masson P; Fayon M; Demarquez JL
Genet Couns; 1991; 2(4):249-53. PubMed ID: 1799426
[TBL] [Abstract][Full Text] [Related]
52. Infantile chronic subdural hematoma of the posterior fossa diagnosed by computerized tomography. Case report.
French BN; Dublin AB
J Neurosurg; 1977 Dec; 47(6):949-52. PubMed ID: 925750
[TBL] [Abstract][Full Text] [Related]
53. [Recurrent chronic subdural hematoma--pachymeningeosis haemorrhagica interna].
Hentschel F
Zentralbl Neurochir; 1990; 51(2):119-23. PubMed ID: 2087888
[TBL] [Abstract][Full Text] [Related]
54. Ocular manifestations of Noonan syndrome.
Marin Lda R; da Silva FT; de Sá LC; Brasil AS; Pereira A; Furquim IM; Kim CA; Bertola DR
Ophthalmic Genet; 2012 Mar; 33(1):1-5. PubMed ID: 21815719
[TBL] [Abstract][Full Text] [Related]
55. Noonan, Costello and cardio-facio-cutaneous syndromes: dysregulation of the Ras-MAPK pathway.
Tidyman WE; Rauen KA
Expert Rev Mol Med; 2008 Dec; 10():e37. PubMed ID: 19063751
[TBL] [Abstract][Full Text] [Related]
56. Is Neurofibromatosis Type 1-Noonan Syndrome a Phenotypic Result of Combined Genetic and Epigenetic Factors?
Yapijakis C; Pachis N; Natsis S; Voumvourakis C
In Vivo; 2016; 30(3):315-20. PubMed ID: 27107091
[TBL] [Abstract][Full Text] [Related]
57. A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation-a review of the literature.
Nemcikova M; Vejvalkova S; Fencl F; Sukova M; Krepelova A
Eur J Pediatr; 2016 Apr; 175(4):587-92. PubMed ID: 26518681
[TBL] [Abstract][Full Text] [Related]
58. A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype?
Maximilian C; Ioan DM; Fryns JP
Genet Couns; 1992; 3(2):115-8. PubMed ID: 1642809
[TBL] [Abstract][Full Text] [Related]
59. [Peculiarities in a subdural hematoma].
Pirker E; Diemath HE
Fortschr Geb Rontgenstr Nuklearmed; 1967 Feb; 106(2):231-5. PubMed ID: 5626679
[No Abstract] [Full Text] [Related]
60. Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association.
Bahuau M; Flintoff W; Assouline B; Lyonnet S; Le Merrer M; Prieur M; Guilloud-Bataille M; Feingold N; Munnich A; Vidaud M; Vidaud D
Am J Med Genet; 1996 Dec; 66(3):347-55. PubMed ID: 8985499
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
