Gambardella S - Search Results

1

Harmonizing Genetic Testing for Parkinson's Disease: Results of the PARKNET Multicentric Study.

Di Fonzo A, Percetti M, Monfrini E, Palmieri I, Albanese A, Avenali M, Bartoletti-Stella A, Blandini F, Brescia G, Calandra-Buonaura G, Campopiano R, Capellari S, Colangelo I, Comi GP, Cuconato G, Ferese R, Galandra C, Gambardella S, Garavaglia B, Gaudio A, Giardina E, Invernizzi F, Mandich P, Mineri R, Panteghini C, Reale C, Trevisan L, Zampatti S, Cortelli P, Valente EM; PARKNET study group. Di Fonzo A, et al. Among authors: gambardella s. Mov Disord. 2023 Dec;38(12):2241-2248. doi: 10.1002/mds.29617. Epub 2023 Sep 26. Mov Disord. 2023. PMID: 37750340 Free article.

2

Gene symbol: ED1. Disease: Ectodermal dysplasia.

Gambardella S. Gambardella S. Hum Genet. 2008 Feb;123(1):103. Hum Genet. 2008. PMID: 18386318 No abstract available.

3

Bone marrow and umbilical cord blood human mesenchymal stem cells: state of the art.

Malgieri A, Kantzari E, Patrizi MP, Gambardella S. Malgieri A, et al. Among authors: gambardella s. Int J Clin Exp Med. 2010 Sep 7;3(4):248-69. Int J Clin Exp Med. 2010. PMID: 21072260 Free PMC article.

4

TREM Receptors Connecting Bowel Inflammation to Neurodegenerative Disorders.

Natale G, Biagioni F, Busceti CL, Gambardella S, Limanaqi F, Fornai F. Natale G, et al. Among authors: gambardella s. Cells. 2019 Sep 21;8(10):1124. doi: 10.3390/cells8101124. Cells. 2019. PMID: 31546668 Free PMC article. Review.

5

Gene expression profile study in CFTR mutated bronchial cell lines.

Gambardella S, Biancolella M, D'Apice MR, Amati F, Sangiuolo F, Farcomeni A, Chillemi G, Bueno S, Desideri A, Novelli G. Gambardella S, et al. Clin Exp Med. 2006 Dec;6(4):157-65. doi: 10.1007/s10238-006-0116-5. Clin Exp Med. 2006. PMID: 17191107

6

New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis ?

Corleto VD, Gambardella S, Gullotta F, D'Apice MR, Piciucchi M, Galli E, Lucidi V, Novelli G, Delle Fave G. Corleto VD, et al. Among authors: gambardella s. BMC Gastroenterol. 2010 Oct 15;10:119. doi: 10.1186/1471-230X-10-119. BMC Gastroenterol. 2010. PMID: 20950468 Free PMC article.

7

Gene symbol: ED1. Disease: Ectodermal dysplasia.

Gambardella S. Gambardella S. Hum Genet. 2008 Feb;123(1):102. Hum Genet. 2008. PMID: 18386314 No abstract available.

8

Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy.

D'Apice MR, Gambardella S, Bengala M, Russo S, Nardone AM, Lucidi V, Sangiuolo F, Novelli G. D'Apice MR, et al. Among authors: gambardella s. BMC Med Genet. 2004 Apr 14;5:8. doi: 10.1186/1471-2350-5-8. BMC Med Genet. 2004. PMID: 15084222 Free PMC article.

9

Phenotypic variability in a family with pancreatitis and cystic fibrosis sharing common mild CFTR mutation: report on CFTR mutations and their phenotypic variability.

Alghisi F, Bella S, Lucidi V, Angioni A, Tomaiuolo AC, D'Apice MR, Gambardella S, Novelli G. Alghisi F, et al. Among authors: gambardella s. Pancreas. 2009 Jan;38(1):109-10. doi: 10.1097/MPA.0b013e3181671b9c. Pancreas. 2009. PMID: 19106752 No abstract available.

10

Denaturing HPLC in laboratory diagnosis of hereditary angioedema.

Guarino MD, Perricone C, Guarino S, Gambardella S, D'Apice MR, Fontana L, Novelli G, Perricone R. Guarino MD, et al. Among authors: gambardella s. J Allergy Clin Immunol. 2007 Oct;120(4):962-5. doi: 10.1016/j.jaci.2007.05.041. Epub 2007 Jul 19. J Allergy Clin Immunol. 2007. PMID: 17659327 No abstract available.

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