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Proceedings of the 14th International Newborn Brain Conference: Fetal and/or neonatal brain development, both normal and abnormal.
Abdi K, Adams E, Agarwal S, Ergun MA, Altamimi T, Aral A, Arfi H, Armour E, Armstrong L, Mulkey SB, Bambi J, Baxter L, Benner E, Bhattacharya S, Biselele T, Bolay H, Mayorga PC, Carrasco M, Carter E, Chao A, Cooke A, Corsi-Cabrera M, Cubero-Rego L, Cuddyer D, Gano DD, Cubero-Rego MLA, de Ribaupierre S, Drobyshevsky A, El-Dib M, Elmazoglu Z, Emrick L, Epstein A, Erdei C, Flynn P, Duerden EG, Gibson K, Gregory S, Topa EGA, Aliyu MH, Harmony T, Harshbarger J, Hartley C, Hayakawa M, Kazan HH, Inder T, Ito Y, Jain V, Jurkiewicz M, Kapoor B, Kebaya L, Keles Gulnerman E, Kidokoro H, Kling E, Kumai S, Lebane D, Lemmon M, Salihu HM, Marchant S, Maxfield C, Mbayabo G, Meyerink P, Millman R, Mitsumatsu T, Nakata T, Narita H, Natsume J, Pacheco J, Pagano L, Pardo A, Peyton C, Pineda R, Reddy S, Ricardo-Garcell J, Rikard B, Roychaudhuri S, Nichols ES, Sadowska-Krawczenko I, Sato Y, Sawamura F, Scher M, Sharon D, Sheldon Y, Shiraki A, Singh E, Steele T, Suzui R, Tady BP, Taga G, Tarui T, Trapp N, Tristao L, Tuka D, Ushida T, Usman F, Venkatesan C, Watanabe H, Witulska-Alagöz A, Yamamoto H, Yarnykh V, Younge N. Abdi K, et al. Among authors: sharon d. J Neonatal Perinatal Med. 2023;16(s1):S1-S19. doi: 10.3233/NPM-239001. J Neonatal Perinatal Med. 2023. PMID: 37599540 No abstract available.
Proceedings of the 14th International Newborn Brain Conference: Neuro-imaging studies.
Herrera S, Herrera S, Cabacungan E, Cohen S, Thyagarajan B, Jefferies K, Avanaki K, Manwar R, McGuire L, Islam T, Shoo A, Charbel FT, Pillers DM, Verschuur A, van Steenis A, Boswinkel V, Nijholt I, Boomsma M, Steggerda S, Meijler G, Leijser L, Park SG, Yang HJ, Lim SY, Kim SH, Shin SH, Kim EK, Kim HS, Shiraki A, Kidokoro H, Watanabe H, Taga G, Narita H, Mitsumatsu T, Kumai S, Suzui R, Sawamura F, Ito Y, Yamamoto H, Nakata T, Sato Y, Hayakawa M, Natsume J, Buchmayer J, Kasprian G, Giordano V, Jernej R, Klebermass-Schrehof K, Berger A, Goeral K, Garvey A, El-Shibiny H, Yang E, Inder T, El-Dib M, Garvey A, Grant E, Manning S, Volpe J, Inder T, Roychaudhuri S, Pineda R, Sharon D, Singh E, Steele T, Sheldon Y, Cuddyer D, Yang E, Erdei C, Szakmar E, Andorka C, Barta H, Sesztak T, Varga E, Szabo M, Jermendy A, Panzarini I, King R, Verschuur AS, Hendson L, Carlson H, Scotland J, Zein H, Mohammed K, Meijler G, Leijser L, Bach A, Lambing H, Rogers EE, Xu D, James BA, Ferriero DM, Glass HC, Gano D, Igreja L, Ferreira A, Gomes R, Sousa B, Novo A, Alves JE, Proença E, Carvalho C. Herrera S, et al. Among authors: sharon d. J Neonatal Perinatal Med. 2023;16(s1):S75-S101. doi: 10.3233/NPM-239005. J Neonatal Perinatal Med. 2023. PMID: 37599544 No abstract available.
Nationwide Prevalence of Inherited Retinal Diseases in the Israeli Population.
Shalom S, Ben-Yosef T, Sher I, Zag A, Rotenstreich Y, Poleg T, Birk OS, Gradstein L, Ehrenberg M, Deitch I, Mezer E, Hecht I, Pras E, Ramon D, Khateb S, Zur D, Newman H, Kharouba R, Goldenberg-Cohen N, Leibu R, Soudry S, Perlman I, Banin E, Sharon D. Shalom S, et al. Among authors: sharon d. JAMA Ophthalmol. 2024 May 16:e241461. doi: 10.1001/jamaophthalmol.2024.1461. Online ahead of print. JAMA Ophthalmol. 2024. PMID: 38753338
Periodic limb movement disorder in children: A systematic review.
DelRosso LM, Picchietti DL, Sharon D, Spruyt K, Owens JA, Walters AS, Zucconi M, Ferri R; International Restless Legs Syndrome Study Group (IRLSSG). DelRosso LM, et al. Among authors: sharon d. Sleep Med Rev. 2024 Apr 16;76:101935. doi: 10.1016/j.smrv.2024.101935. Online ahead of print. Sleep Med Rev. 2024. PMID: 38652932 Review.
Representation of Women Among Individuals With Mild Variants in ABCA4-Associated Retinopathy: A Meta-Analysis.
Cornelis SS, IntHout J, Runhart EH, Grunewald O, Lin S, Corradi Z, Khan M, Hitti-Malin RJ, Whelan L, Farrar GJ, Sharon D, van den Born LI, Arno G, Simcoe M, Michaelides M, Webster AR, Roosing S, Mahroo OA, Dhaenens CM, Cremers FPM; Study Group. Cornelis SS, et al. Among authors: sharon d. JAMA Ophthalmol. 2024 May 1;142(5):463-471. doi: 10.1001/jamaophthalmol.2024.0660. JAMA Ophthalmol. 2024. PMID: 38602673
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes.
Hitti-Malin RJ, Panneman DM, Corradi Z, Boonen EGM, Astuti G, Dhaenens CM, Stöhr H, Weber BHF, Sharon D, Banin E, Karali M, Banfi S, Ben-Yosef T, Glavač D, Farrar GJ, Ayuso C, Liskova P, Dudakova L, Vajter M, Ołdak M, Szaflik JP, Matynia A, Gorin MB, Kämpjärvi K, Bauwens M, De Baere E, Hoyng CB, Li CHZ, Klaver CCW, Inglehearn CF, Fujinami K, Rivolta C, Allikmets R, Zernant J, Lee W, Podhajcer OL, Fakin A, Sajovic J, AlTalbishi A, Valeina S, Taurina G, Vincent AL, Roberts L, Ramesar R, Sartor G, Luppi E, Downes SM, van den Born LI, McLaren TL, De Roach JN, Lamey TM, Thompson JA, Chen FK, Tracewska AM, Kamakari S, Sallum JMF, Bolz HJ, Kayserili H, Roosing S, Cremers FPM. Hitti-Malin RJ, et al. Among authors: sharon d. Biomolecules. 2024 Mar 19;14(3):367. doi: 10.3390/biom14030367. Biomolecules. 2024. PMID: 38540785 Free PMC article.
Fine-tuning FAM161A gene augmentation therapy to restore retinal function.
Arsenijevic Y, Chang N, Mercey O, El Fersioui Y, Koskiniemi-Kuendig H, Joubert C, Bemelmans AP, Rivolta C, Banin E, Sharon D, Guichard P, Hamel V, Kostic C. Arsenijevic Y, et al. Among authors: sharon d. EMBO Mol Med. 2024 Apr;16(4):805-822. doi: 10.1038/s44321-024-00053-x. Epub 2024 Mar 19. EMBO Mol Med. 2024. PMID: 38504136 Free PMC article.
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration.
Han JH, Rodenburg K, Hayman T, Calzetti G, Kaminska K, Quinodoz M, Marra M, Wallerich S, Allon G, Nagy ZZ, Knézy K, Li Y, Chen R, Barboni MTS, Yang P, Pennesi ME, van den Born LI, Varsányi B, Szabó V, Sharon D, Banin E, Ben-Yosef T, Roosing S, Koenekoop RK, Rivolta C. Han JH, et al. Among authors: sharon d. Genet Med. 2024 Feb 28:101106. doi: 10.1016/j.gim.2024.101106. Online ahead of print. Genet Med. 2024. PMID: 38420906 Free article.
299 results