Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

70 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Adherence to guidelines for management of children hospitalized for acute diarrhea.
Lo Vecchio A, Liguoro I, Bruzzese D, Scotto R, Parola L, Gargantini G, Guarino A; Accreditation and Quality Improvement Working Group of Italian Society of Pediatrics. Lo Vecchio A, et al. Pediatr Infect Dis J. 2014 Nov;33(11):1103-8. doi: 10.1097/INF.0000000000000396. Pediatr Infect Dis J. 2014. PMID: 24830697
Correction: Biobank for craniosynostosis and faciocraniosynostosis, rare pediatric congenital craniofacial disorders: a study protocol.
De Martino L, Mirabelli P, Quaglietta L, Ferrara UP, Picariello S, De Gennaro DV, Aiello M, Smaldone G, Aliberti F, Spennato P, De Brasi D, Covelli E, Cinalli G. De Martino L, et al. Among authors: de brasi d. Childs Nerv Syst. 2024 Nov;40(11):3701. doi: 10.1007/s00381-024-06625-z. Childs Nerv Syst. 2024. PMID: 39311931 Free PMC article. No abstract available.
Biobank for craniosynostosis and faciocraniosynostosis, rare pediatric congenital craniofacial disorders: a study protocol.
De Martino L, Mirabelli P, Quaglietta L, Ferrara UP, Picariello S, De Gennaro DV, Aiello M, Smaldone G, Aliberti F, Spennato P, De Brasi D, Covelli E, Cinalli G. De Martino L, et al. Among authors: de brasi d. Childs Nerv Syst. 2024 Nov;40(11):3693-3700. doi: 10.1007/s00381-024-06555-w. Epub 2024 Aug 12. Childs Nerv Syst. 2024. PMID: 39133244 Free PMC article.
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?
Pignata L, Cecere F, Acquaviva F, D'Angelo E, Cioffi D, Pellino V, Palumbo O, Palumbo P, Carella M, Sparago A, De Brasi D, Cerrato F, Riccio A. Pignata L, et al. Among authors: de brasi d. Front Cell Dev Biol. 2023 Aug 10;11:1237629. doi: 10.3389/fcell.2023.1237629. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 37635873 Free PMC article.
De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling.
Morleo M, Venditti R, Theodorou E, Briere LC, Rosello M, Tirozzi A, Tammaro R, Al-Badri N, High FA, Shi J; Undiagnosed Diseases Network; Telethon Undiagnosed Diseases Program; Putti E, Ferrante L, Cetrangolo V, Torella A, Walker MA, Tenconi R, Iascone M, Mei D, Guerrini R, van der Smagt J, Kroes HY, van Gassen KLI, Bilal M, Umair M, Pingault V, Attie-Bitach T, Amiel J, Ejaz R, Rodan L, Zollino M, Agrawal PB, Del Bene F, Nigro V, Sweetser DA, Franco B. Morleo M, et al. Am J Hum Genet. 2023 Aug 3;110(8):1377-1393. doi: 10.1016/j.ajhg.2023.06.012. Epub 2023 Jul 13. Am J Hum Genet. 2023. PMID: 37451268 Free PMC article.
CHAMP1-related disorders: pathomechanisms triggered by different genomic alterations define distinct nosological categories.
Amenta S, Marangi G, Orteschi D, Frangella S, Gurrieri F, Paccagnella E; Telethon Undiagnosed Diseases Program (TUDP) Study Group; Scala M, Romano F, Capra V, Nigro V, Zollino M. Amenta S, et al. Eur J Hum Genet. 2023 Jun;31(6):648-653. doi: 10.1038/s41431-023-01305-z. Epub 2023 Feb 16. Eur J Hum Genet. 2023. PMID: 36797464 Free PMC article. Review.
70 results