Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
5 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
ETIOLOGIES OF INFECTIONS IN DIABETIC PATIENTS HOSPITALIZED AT BOUAKE UNIVERTY TEACHING HOSPITAL, CÔTE D'IVOIRE.
Afr J Infect Dis. 2023 Aug 1;17(2 Suppl):1-5. doi: 10.21010/Ajidv17i2S.1. eCollection 2023.
Afr J Infect Dis. 2023.
PMID: 37822552
Free PMC article.
SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance.
Cordovado A, Schaettin M, Jeanne M, Panasenkava V, Denommé-Pichon AS, Keren B, Mignot C, Doco-Fenzy M, Rodan L, Ramsey K, Narayanan V, Jones JR, Prijoles EJ, Mitchell WG, Ozmore JR, Juliette K, Torti E, Normand EA, Granger L, Petersen AK, Au MG, Matheny JP, Phornphutkul C, Chambers MK, Fernández-Ramos JA, López-Laso E, Kruer MC, Bakhtiari S, Zollino M, Morleo M, Marangi G, Mei D, Pisano T, Guerrini R, Louie RJ, Childers A, Everman DB, Isidor B, Audebert-Bellanger S, Odent S, Bonneau D, Gilbert-Dussardier B, Redon R, Bézieau S, Laumonnier F, Stoeckli ET, Toutain A, Vuillaume ML.
Cordovado A, et al. Among authors: juliette k.
Hum Mol Genet. 2022 Sep 29;31(19):3325-3340. doi: 10.1093/hmg/ddac114.
Hum Mol Genet. 2022.
PMID: 35604360
Free PMC article.
Item in Clipboard
Parental Perspectives Regarding the Impact of the COVID-19 Pandemic on Their Children.
Tanti S, Troost JP, Samuels E, Mckay A, Kowalski-Dobson T, Vereen D, Gorka N, Nambiar V, Key K, Campbell B, Greene-Moton E, Evans L, Bailey S, Juliette K, Sparks A, DeLoney EH, Piechowski P, Woolford SJ.
Tanti S, et al. Among authors: juliette k.
Child Obes. 2023 Jan;19(1):34-45. doi: 10.1089/chi.2021.0216. Epub 2022 Apr 21.
Child Obes. 2023.
PMID: 35447044
Free PMC article.
Item in Clipboard
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.
Kour S, Rajan DS, Fortuna TR, Anderson EN, Ward C, Lee Y, Lee S, Shin YB, Chae JH, Choi M, Siquier K, Cantagrel V, Amiel J, Stolerman ES, Barnett SS, Cousin MA, Castro D, McDonald K, Kirmse B, Nemeth AH, Rajasundaram D, Innes AM, Lynch D, Frosk P, Collins A, Gibbons M, Yang M, Desguerre I, Boddaert N, Gitiaux C, Rydning SL, Selmer KK, Urreizti R, Garcia-Oguiza A, Osorio AN, Verdura E, Pujol A, McCurry HR, Landers JE, Agnihotri S, Andriescu EC, Moody SB, Phornphutkul C, Sacoto MJG, Begtrup A, Houlden H, Kirschner J, Schorling D, Rudnik-Schöneborn S, Strom TM, Leiz S, Juliette K, Richardson R, Yang Y, Zhang Y, Wang M, Wang J, Wang X, Platzer K, Donkervoort S, Bönnemann CG, Wagner M, Issa MY, Elbendary HM, Stanley V, Maroofian R, Gleeson JG, Zaki MS, Senderek J, Pandey UB.
Kour S, et al. Among authors: juliette k.
Nat Commun. 2021 May 7;12(1):2558. doi: 10.1038/s41467-021-22627-w.
Nat Commun. 2021.
PMID: 33963192
Free PMC article.
Item in Clipboard
Clinical diagnostic exome sequencing in dystonia: Genetic testing challenges for complex conditions.
Powis Z, Towne MC, Hagman KDF, Blanco K, Palmaer E, Castro A, Sajan SA, Radtke K, Feyma TJ, Juliette K, Tang S, Sidiropoulos C.
Powis Z, et al. Among authors: juliette k.
Clin Genet. 2020 Feb;97(2):305-311. doi: 10.1111/cge.13657. Epub 2019 Oct 30.
Clin Genet. 2020.
PMID: 31628766
Item in Clipboard
Cite
Cite