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2013 1
2014 2
2019 2
2020 1
2021 2
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Page 1
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder.
Carapito R, Ivanova EL, Morlon A, Meng L, Molitor A, Erdmann E, Kieffer B, Pichot A, Naegely L, Kolmer A, Paul N, Hanauer A, Tran Mau-Them F, Jean-Marçais N, Hiatt SM, Cooper GM, Tvrdik T, Muir AM, Dimartino C, Chopra M, Amiel J, Gordon CT, Dutreux F, Garde A, Thauvin-Robinet C, Wang X, Leduc MS, Phillips M, Crawford HP, Kukolich MK, Hunt D, Harrison V, Kharbanda M; Deciphering Developmental Disorders Study; University of Washington Center for Mendelian Genomics, Smigiel R, Gold N, Hung CY, Viskochil DH, Dugan SL, Bayrak-Toydemir P, Joly-Helas G, Guerrot AM, Schluth-Bolard C, Rio M, Wentzensen IM, McWalter K, Schnur RE, Lewis AM, Lalani SR, Mensah-Bonsu N, Céraline J, Sun Z, Ploski R, Bacino CA, Mefford HC, Faivre L, Bodamer O, Chelly J, Isidor B, Bahram S. Carapito R, et al. Among authors: mensah bonsu n. Am J Hum Genet. 2019 Feb 7;104(2):319-330. doi: 10.1016/j.ajhg.2018.12.007. Epub 2019 Jan 10. Am J Hum Genet. 2019. PMID: 30639322 Free PMC article.
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder.
Carapito R, Ivanova EL, Morlon A, Meng L, Molitor A, Erdmann E, Kieffer B, Pichot A, Naegely L, Kolmer A, Paul N, Hanauer A, Tran Mau-Them F, Jean-Marçais N, Hiatt SM, Cooper GM, Tvrdik T, Muir AM, Dimartino C, Chopra M, Amiel J, Gordon CT, Dutreux F, Garde A, Thauvin-Robinet C, Wang X, Leduc MS, Phillips M, Crawford HP, Kukolich MK, Hunt D, Harrison V, Kharbanda M; Deciphering Developmental Disorders Study; University of Washington Center for Mendelian Genomics, Smigiel R, Gold N, Hung CY, Viskochil DH, Dugan SL, Bayrak-Toydemir P, Joly-Helas G, Guerrot AM, Schluth-Bolard C, Rio M, Wentzensen IM, McWalter K, Schnur RE, Lewis AM, Lalani SR, Mensah-Bonsu N, Céraline J, Sun Z, Ploski R, Bacino CA, Mefford HC, Faivre L, Bodamer O, Chelly J, Isidor B, Bahram S. Carapito R, et al. Among authors: mensah bonsu n. Am J Hum Genet. 2020 Jan 2;106(1):137. doi: 10.1016/j.ajhg.2019.11.014. Epub 2019 Dec 24. Am J Hum Genet. 2020. PMID: 31879022 Free PMC article. No abstract available.
Diffuse cutaneous mastocytosis, bullous variant, presenting in a six-month-old infant.
Kinneman L, Molloy B, Nguyen V, Loizou D, Silverman R, Mensah-Bonsu N, Enav B, Johal J, Plassmeyer M, Ryherd M, Austin L, Limgala R, Brown M, Gupta R, Noonan L, Hider P, Alpan O. Kinneman L, et al. Among authors: mensah bonsu n. J Allergy Clin Immunol Pract. 2014 May-Jun;2(3):341-2. doi: 10.1016/j.jaip.2014.02.016. J Allergy Clin Immunol Pract. 2014. PMID: 24811027 No abstract available.
The Impact of Asymptomatic Congenital Cytomegalovirus on Adult Quality of Life.
Katusic MZ, Mensah-Bonsu NE, Miller JA, Turcich MR, Iovino I, Vinson-Sellers S, Voigt RG, Demmler-Harrison GJ; Houston Congenital CMV Longitudinal Study. Katusic MZ, et al. Among authors: mensah bonsu ne. J Dev Behav Pediatr. 2021 Jan 1;42(1):46-54. doi: 10.1097/DBP.0000000000000843. J Dev Behav Pediatr. 2021. PMID: 33055522
The curious case of ileocolic intussusception.
Teo WY, Kim S, Mensah-Bonsu N. Teo WY, et al. Among authors: mensah bonsu n. J Paediatr Child Health. 2014 Jul;50(7):573-4. doi: 10.1111/jpc.12664. J Paediatr Child Health. 2014. PMID: 25041299 No abstract available.
Index of suspicion. Case 1: abdominal pain, distension, hard stool, and diarrhea in an 11-year-old boy. Case 2: recurrent otitis media in a 4-year-old boy. Case 3: gynecomastia and galactorrhea in a 15-year-old boy.
Young S, Joseph-Griffin M, Mensah-Bonsu N, Hageman JR, Schwartz D, Mikita C, Luca P, Urbach S. Young S, et al. Among authors: mensah bonsu n. Pediatr Rev. 2013 Jul;34(7):322-7. doi: 10.1542/pir.34-7-322. Pediatr Rev. 2013. PMID: 23818086 No abstract available.