130 related articles for article (PubMed ID: 38847235)
1. Noonan syndrome and type 1 Chiari malformation: Possible association.
Samuels M; Northrup H
Am J Med Genet A; 2024 Jun; ():e63776. PubMed ID: 38847235
[TBL] [Abstract][Full Text] [Related]
2. Molecular and clinical profile of patients referred as Noonan or Noonan-like syndrome in Greece: a cohort of 86 patients.
Papadopoulos G; Papadopoulou A; Kosma K; Papadimitriou A; Papaevangelou V; Kanaka-Gantenbein C; Bountouvi E; Kitsiou-Tzeli S
Eur J Pediatr; 2022 Oct; 181(10):3691-3700. PubMed ID: 35904599
[TBL] [Abstract][Full Text] [Related]
3. The Chiari pseudotumor cerebri syndrome: symptom recurrence after decompressive surgery for Chiari malformation type I.
Fagan LH; Ferguson S; Yassari R; Frim DM
Pediatr Neurosurg; 2006; 42(1):14-9. PubMed ID: 16357496
[TBL] [Abstract][Full Text] [Related]
4. Posterior cranial fossa and cervical spine morphometric abnormalities in symptomatic Chiari type 0 and Chiari type 1 malformation patients with and without syringomyelia.
Bogdanov EI; Faizutdinova AT; Heiss JD
Acta Neurochir (Wien); 2021 Nov; 163(11):3051-3064. PubMed ID: 34448046
[TBL] [Abstract][Full Text] [Related]
5. The Small Posterior Cranial Fossa Syndrome and Chiari Malformation Type 0.
Bogdanov EI; Faizutdinova AT; Heiss JD
J Clin Med; 2022 Sep; 11(18):. PubMed ID: 36143119
[TBL] [Abstract][Full Text] [Related]
6. Association between Noonan syndrome and Chiari I malformation: a case-based update.
Keh YS; Abernethy L; Pettorini B
Childs Nerv Syst; 2013 May; 29(5):749-52. PubMed ID: 23239255
[TBL] [Abstract][Full Text] [Related]
7. Onset of Chiari type 1 malformation: insights from a small series of intrauterine MR imaging cases.
Palumbo G; Arrigoni F; Peruzzo D; Parazzini C; D'Errico I; Agazzi GM; Pinelli L; Triulzi F; Righini A
Neuroradiology; 2023 Sep; 65(9):1387-1394. PubMed ID: 37329352
[TBL] [Abstract][Full Text] [Related]
8. [Arnold-Chiari malformation in Noonan syndrome and other syndromes of the RAS/MAPK pathway].
Ejarque I; Millán-Salvador JM; Oltra S; Pesudo-Martínez JV; Beneyto M; Pérez-Aytés A
Rev Neurol; 2015 May; 60(9):408-12. PubMed ID: 25912702
[TBL] [Abstract][Full Text] [Related]
9. Epidemiology of Symptomatic Chiari Malformation in Tatarstan: Regional and Ethnic Differences in Prevalence.
Bogdanov EI; Faizutdinova AT; Mendelevich EG; Sozinov AS; Heiss JD
Neurosurgery; 2019 May; 84(5):1090-1097. PubMed ID: 29788393
[TBL] [Abstract][Full Text] [Related]
10. [Clinical and radiological rationale for distinguishing subtypes of primary Chiari I malformation].
Faizutdinova АТ; Bogdanov EI
Zh Nevrol Psikhiatr Im S S Korsakova; 2020; 120(8):64-69. PubMed ID: 32929926
[TBL] [Abstract][Full Text] [Related]
11. Clinical Variability in a Family with Noonan Syndrome with a Homozygous
Yıldırım R; Unal E; Özalkak Ş; Akalın A; Aykut A; Yılmaz N
J Clin Res Pediatr Endocrinol; 2024 Mar; 16(1):76-83. PubMed ID: 37847107
[TBL] [Abstract][Full Text] [Related]
12. Hemifacial spasm secondary to Chiari malformation type I: Systematic review with case illustration.
Hunsaker JC; Baker CM; Schmidt RH; Rahimpour S
J Clin Neurosci; 2022 Jul; 101():21-25. PubMed ID: 35512425
[TBL] [Abstract][Full Text] [Related]
13. Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship.
Massimi L; Palombi D; Contaldo I; Veredice C; Chieffo DRP; Calandrelli R; Tamburrini G; Battaglia DI
J Clin Med; 2022 Oct; 11(20):. PubMed ID: 36294502
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Management of failed Chiari decompression and intrasyringeal hemorrhage in Noonan syndrome: illustrative cases.
Falls CJ; Page PS; Greeneway GP; Resnick DK; Stadler JA
J Neurosurg Case Lessons; 2022 Jan; 3(4):. PubMed ID: 36130568
[TBL] [Abstract][Full Text] [Related]
16. Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing.
Musolf AM; Ho WSC; Long KA; Zhuang Z; Argersinger DP; Sun H; Moiz BA; Simpson CL; Mendelevich EG; Bogdanov EI; Bailey-Wilson JE; Heiss JD
Eur J Hum Genet; 2019 Oct; 27(10):1599-1610. PubMed ID: 31227808
[TBL] [Abstract][Full Text] [Related]
17. Predictive Factors of Headache Resolution After Chiari Type 1 Malformation Surgery.
Grangeon L; Puy L; Gilard V; Hebant B; Langlois O; Derrey S; Gerardin E; Maltete D; Guegan-Massardier E; Magne N
World Neurosurg; 2018 Feb; 110():e60-e66. PubMed ID: 29066319
[TBL] [Abstract][Full Text] [Related]
18. High frequency of hotspot mutation in PTPN11 gene among Moroccan patients with Noonan syndrome.
Ouboukss F; Adadi N; Amasdl S; Smaili W; Laarabi FZ; Lyahyai J; Sefiani A; Ratbi I
J Appl Genet; 2024 May; 65(2):303-308. PubMed ID: 37987971
[TBL] [Abstract][Full Text] [Related]
19. Migraine in Chiari 1 Malformation: a cross-sectional, single centre study.
Ciaramitaro P; Rota E; Ferraris M; Stura I; Migliaretti G; Cocito D
Acta Neurol Belg; 2022 Aug; 122(4):947-954. PubMed ID: 34047952
[TBL] [Abstract][Full Text] [Related]
20. Differences in severity of cardiovascular anomalies in children with Noonan syndrome based on the causative gene.
Shehade-Awwad N; Yeshayahu Y; Pinhas-Hamiel O; Katz U
Front Pediatr; 2022; 10():946071. PubMed ID: 36160796
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]