158 related articles for article (PubMed ID: 33352116)
1. Rare and de novo coding variants in chromodomain genes in Chiari I malformation.
Sadler B; Wilborn J; Antunes L; Kuensting T; Hale AT; Gannon SR; McCall K; Cruchaga C; Harms M; Voisin N; Reymond A; Cappuccio G; Brunetti-Pierri N; Tartaglia M; Niceta M; Leoni C; Zampino G; Ashley-Koch A; Urbizu A; Garrett ME; Soldano K; Macaya A; Conrad D; Strahle J; Dobbs MB; Turner TN; Shannon CN; Brockmeyer D; Limbrick DD; Gurnett CA; Haller G
Am J Hum Genet; 2021 Jan; 108(1):100-114. PubMed ID: 33352116
[TBL] [Abstract][Full Text] [Related]
2. Human genetics and molecular genomics of Chiari malformation type 1.
Mekbib KY; Muñoz W; Allington G; McGee S; Mehta NH; Shofi JP; Fortes C; Le HT; Nelson-Williams C; Nanda P; Dennis E; Kundishora AJ; Khanna A; Smith H; Ocken J; Greenberg ABW; Wu R; Moreno-De-Luca A; DeSpenza T; Zhao S; Marlier A; Jin SC; Alper SL; Butler WE; Kahle KT
Trends Mol Med; 2023 Dec; 29(12):1059-1075. PubMed ID: 37802664
[TBL] [Abstract][Full Text] [Related]
3. Clinical diagnosis-part I: what is really caused by Chiari I.
Ciaramitaro P; Ferraris M; Massaro F; Garbossa D
Childs Nerv Syst; 2019 Oct; 35(10):1673-1679. PubMed ID: 31161267
[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. [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]
6. A genetic hypothesis for Chiari I malformation with or without syringomyelia.
Speer MC; George TM; Enterline DS; Franklin A; Wolpert CM; Milhorat TH
Neurosurg Focus; 2000 Mar; 8(3):E12. PubMed ID: 16676924
[TBL] [Abstract][Full Text] [Related]
7. [Treatment of syringomyelia associated with Chiari 1 malformation].
Zuev AA; Kostenko GV
Zh Nevrol Psikhiatr Im S S Korsakova; 2017; 117(3):102-106. PubMed ID: 28399105
[TBL] [Abstract][Full Text] [Related]
8. Long-term outcomes for children with an incidentally discovered Chiari malformation type 1: what is the clinical significance?
Davidson L; Phan TN; Myseros JS; Magge SN; Oluigbo C; Sanchez CE; Keating RF
Childs Nerv Syst; 2021 Apr; 37(4):1191-1197. PubMed ID: 33230572
[TBL] [Abstract][Full Text] [Related]
9. Elucidating the Genetic Basis of Chiari I Malformation.
Haller G; Sadler B
Neurosurg Clin N Am; 2023 Jan; 34(1):55-60. PubMed ID: 36424064
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type I reveals candidate genes for cranio-facial development.
Merello E; Tattini L; Magi A; Accogli A; Piatelli G; Pavanello M; Tortora D; Cama A; Kibar Z; Capra V; De Marco P
Eur J Hum Genet; 2017 Aug; 25(8):952-959. PubMed ID: 28513615
[TBL] [Abstract][Full Text] [Related]
13. Cough syncope and hyperventilation-induced convulsion in Chiari 1.5 malformation.
Sasaki R; Shimokawara T; Nagata K; Kinoshita M; Hirabayashi H; Nakase H
Neurol Sci; 2021 May; 42(5):2069-2073. PubMed ID: 33389244
[TBL] [Abstract][Full Text] [Related]
14. Rare functional genetic variants in COL7A1, COL6A5, COL1A2 and COL5A2 frequently occur in Chiari Malformation Type 1.
Urbizu A; Garrett ME; Soldano K; Drechsel O; Loth D; Marcé-Grau A; Mestres I Soler O; Poca MA; Ossowski S; Macaya A; Loth F; Labuda R; Ashley-Koch A
PLoS One; 2021; 16(5):e0251289. PubMed ID: 33974636
[TBL] [Abstract][Full Text] [Related]
15. Amyotrophic Lateral Sclerosis Mimic Syndrome in a 24-Year-Old Man with Chiari 1 Malformation and Syringomyelia: A Clinical Case.
Al-Zamil M; Shnayder NA; Davydova TK; Nasyrova RF; Trefilova VV; Narodova EA; Petrova MM; Romanova IV; Chumakova GA
J Clin Med; 2023 Apr; 12(8):. PubMed ID: 37109269
[TBL] [Abstract][Full Text] [Related]
16. Chiari I malformation with and without basilar invagination: a comparative study.
Klekamp J
Neurosurg Focus; 2015 Apr; 38(4):E12. PubMed ID: 25828488
[TBL] [Abstract][Full Text] [Related]
17. Syringomyelia associated with Chiari I malformation.
Lucchetta M; Cagnin A; Calderone M; Manara R; Rotilio A; Briani C
Neurol Sci; 2009 Dec; 30(6):525-6. PubMed ID: 19768371
[TBL] [Abstract][Full Text] [Related]
18. Syringomyelia in twin brothers discordant for Chiari I malformation: case report.
Tubbs RS; Wellons JC; Blount JP; Oakes WJ
J Child Neurol; 2004 Jun; 19(6):459-62. PubMed ID: 15449382
[TBL] [Abstract][Full Text] [Related]
19. Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin-Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing.
Lu G; Peng Q; Wu L; Zhang J; Ma L
BMC Med Genomics; 2021 Nov; 14(1):270. PubMed ID: 34775996
[TBL] [Abstract][Full Text] [Related]
20. Postural control in Chiari I malformation: protocol for a paediatric prospective, observational cohort - potential role of posturography for surgical indication.
Stella I; Remen T; Petel A; Joud A; Klein O; Perrin P
BMJ Open; 2022 May; 12(5):e056647. PubMed ID: 35551083
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]