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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2010 | 1 |
2017 | 1 |
2019 | 1 |
2021 | 3 |
2022 | 2 |
2023 | 1 |
Search Results
7
results
Results by year
Page 1
Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome.
Pediatr Neurol. 2022 Jan;126:65-73. doi: 10.1016/j.pediatrneurol.2021.10.008. Epub 2021 Oct 18.
Pediatr Neurol. 2022.
PMID: 34740135
Free article.
New Cohort of Patients With CEDNIK Syndrome Expands the Phenotypic and Genotypic Spectra.
Mah-Som AY, Skrypnyk C, Guerin A, Seroor Jadah RH, Vardhan VN, McKinstry RC, Shinawi MS.
Mah-Som AY, et al. Among authors: shinawi ms.
Neurol Genet. 2021 Jan 12;7(1):e553. doi: 10.1212/NXG.0000000000000553. eCollection 2021 Feb.
Neurol Genet. 2021.
PMID: 33977139
Free PMC article.
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Birth Defects Among 788 Children Born to Gulf War Veterans Based on Physical Examination.
Shinawi MS, Alpern R, Toomey R, Dannenfeldt DS, Reda DJ, Blanchard M.
Shinawi MS, et al.
J Occup Environ Med. 2019 Apr;61(4):263-270. doi: 10.1097/JOM.0000000000001508.
J Occup Environ Med. 2019.
PMID: 30489351
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Novel exon-skipping variant disrupting the basic domain of HCFC1 causes intellectual disability without metabolic abnormalities in both male and female patients.
Wongkittichote P, Wegner DJ, Shinawi MS.
Wongkittichote P, et al. Among authors: shinawi ms.
J Hum Genet. 2021 Jul;66(7):717-724. doi: 10.1038/s10038-020-00892-9. Epub 2021 Jan 30.
J Hum Genet. 2021.
PMID: 33517344
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Prevalence of Semicircular Canal Hypoplasia in Patients With CHARGE Syndrome: 3C Syndrome.
Wineland A, Menezes MD, Shimony JS, Shinawi MS, Hullar TE, Hirose K.
Wineland A, et al. Among authors: shinawi ms.
JAMA Otolaryngol Head Neck Surg. 2017 Feb 1;143(2):168-177. doi: 10.1001/jamaoto.2016.3175.
JAMA Otolaryngol Head Neck Surg. 2017.
PMID: 27832265
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Clinical and biochemical improvement of very long-chain acyl-CoA dehydrogenase deficiency in pregnancy.
Mendez-Figueroa H, Shchelochkov OA, Shaibani A, Aagaard-Tillery K, Shinawi MS.
Mendez-Figueroa H, et al. Among authors: shinawi ms.
J Perinatol. 2010 Aug;30(8):558-62. doi: 10.1038/jp.2009.198.
J Perinatol. 2010.
PMID: 20668464
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Expanding allelic and phenotypic spectrum of ZC4H2-related disorder: A novel hypomorphic variant and high prevalence of tethered cord.
Wongkittichote P, Choi TI, Kim OH, Riley K, Koeberl D, Narayanan V, Ramsey K, Balak C, Schwartz CE, Cueto-Gonzalez AM, Casadesus FM, Kim CH, Shinawi MS.
Wongkittichote P, et al. Among authors: shinawi ms.
Clin Genet. 2023 Feb;103(2):167-178. doi: 10.1111/cge.14248. Epub 2022 Oct 31.
Clin Genet. 2023.
PMID: 36250278
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