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

220 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients.
Garavelli L, Ivanovski I, Caraffi SG, Santodirocco D, Pollazzon M, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Baldo C, Bayat A, Belligni E, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, Devriendt K, Dinulos MB, Djuric O, Epifanio R, Faravelli F, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Lacombe D, Maggi M, Malbora B, Mammi I, Moutton S, Møller R, Muschke P, Napoli M, Pantaleoni C, Pascarella R, Pellicciari A, Poch-Olive ML, Raviglione F, Rivieri F, Russo C, Savasta S, Scarano G, Selicorni A, Silengo M, Sorge G, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zollino M, Dobyns WB, Paciorkowski AR. Garavelli L, et al. Among authors: pascarella r. Genet Med. 2017 Jun;19(6):691-700. doi: 10.1038/gim.2016.176. Epub 2016 Nov 10. Genet Med. 2017. PMID: 27831545 Free PMC article.
Bi-allelic variants in the ESAM tight-junction gene cause a neurodevelopmental disorder associated with fetal intracranial hemorrhage.
Lecca M, Pehlivan D, Suñer DH, Weiss K, Coste T, Zweier M, Oktay Y, Danial-Farran N, Rosti V, Bonasoni MP, Malara A, Contrò G, Zuntini R, Pollazzon M, Pascarella R, Neri A, Fusco C, Marafi D, Mitani T, Posey JE, Bayramoglu SE, Gezdirici A, Hernandez-Rodriguez J, Cladera EA, Miravet E, Roldan-Busto J, Ruiz MA, Bauzá CV, Ben-Sira L, Sigaudy S, Begemann A, Unger S, Güngör S, Hiz S, Sonmezler E, Zehavi Y, Jerdev M, Balduini A, Zuffardi O, Horvath R, Lochmüller H, Rauch A, Garavelli L, Tournier-Lasserve E, Spiegel R, Lupski JR, Errichiello E. Lecca M, et al. Among authors: pascarella r. Am J Hum Genet. 2023 Apr 6;110(4):681-690. doi: 10.1016/j.ajhg.2023.03.005. Epub 2023 Mar 29. Am J Hum Genet. 2023. PMID: 36996813 Free PMC article.
The Ethnic/Racial Variations of Intracerebral Hemorrhage Genetics (ERICH-GENE) Study Protocol.
Falcone GJ, Wolfe SQ, Zedde M, Pascarella R, Jimenez-Conde J, Vallverdu Prats M, Jimenez-Balado J, Pezzini A, Rossi S, Al-Shahi Salman R, Samarasekera N, Zand R, Li J, Jern C, Strbian D, Tomppo L, Sallinen H, Hernandez Guillamon M, Selim M, Owolabi M, Akinyemi R, Fakunle G, Lee TH, Werring D, Hostettler IC, Houlden H, Sharma P, John I, Ken-Dror G, Jenkins W, Sheth KN, Sansing LH, Sanghera DK, Sidorov E, Fernandez-Cadenas I, Cárcel-Márquez J, Chen CJ, Becerril-Gaitan A, Lee KJ, Bae HJ, Dichgans M, Malik R, Debette S, Mishra A, Pare G, Chong M, Kamatani Y, Chen Z, Walters RG, Seshadri S, Fornage M, Sudlow C, Gilkerson LA, Khandwala VJ, Maloney TC, Demel S, Parodi L, Zand R, Nyquist P, Ziai W, Worrall B, Achala VM, Langefeld CD, Rosand J, Anderson CD, Woo D; ERICH-Gene Investigators. Falcone GJ, et al. Among authors: pascarella r. medRxiv [Preprint]. 2025 Jun 13:2025.06.11.25329301. doi: 10.1101/2025.06.11.25329301. medRxiv. 2025. PMID: 40585153 Free PMC article. Preprint.
Carotid reconstitution in chronic dissection.
Zedde M, Romano DG, Valvassori L, Pascarella R. Zedde M, et al. Among authors: pascarella r. Neurol Sci. 2025 May 21. doi: 10.1007/s10072-025-08242-3. Online ahead of print. Neurol Sci. 2025. PMID: 40397307 No abstract available.
220 results