Gandullia P - Search Results

1

Clinical Course of Very Early-Onset Inflammatory Bowel Disease.

Cucinotta U, Arrigo S, Dipasquale V, Gramaglia SMC, Laganà F, Romano C, Gandullia P. Cucinotta U, et al. Among authors: gandullia p. J Pediatr Gastroenterol Nutr. 2023 May 1;76(5):590-595. doi: 10.1097/MPG.0000000000003730. Epub 2023 Feb 7. J Pediatr Gastroenterol Nutr. 2023. PMID: 36754082

2

Epileptic Encephalopathy, Myoclonus-Dystonia, and Premature Pubarche in Siblings with a Novel C-Terminal Truncating Mutation in ATRX Gene.

Giacomini T, Vari MS, Janis S, Prato G, Pisciotta L, Rocchi A, Michelucci A, Di Rocco M, Gandullia P, Mattioli G, Sacco O, Morana G, Mancardi MM. Giacomini T, et al. Among authors: gandullia p. Neuropediatrics. 2019 Oct;50(5):327-331. doi: 10.1055/s-0039-1692141. Epub 2019 Jul 18. Neuropediatrics. 2019. PMID: 31319423

3

Identification of ring Y chromosome: cytogenetic analysis, Southern blot and fluorescent in situ hybridization.

Pezzolo A, Perroni L, Gimelli G, Arslanian A, Porta S, Gandullia P, Gandullia E. Pezzolo A, et al. Among authors: gandullia p, gandullia e. Ann Genet. 1993;36(2):121-5. Ann Genet. 1993. PMID: 8215218

4

Intracranial calcifications and nephrogenic diabetes insipidus.

Di Rocco M, Picco P, Gandullia P, Borrone C. Di Rocco M, et al. Among authors: gandullia p. Eur J Pediatr. 1991 Jun;150(8):599-600. doi: 10.1007/BF02072216. Eur J Pediatr. 1991. PMID: 1954968 No abstract available.

5

Tubulopathy, endocrinopathies and encephalomyopathy in a child with a novel large-scale mitochondrial DNA deletion.

Bruno C, Gandullia P, Santorelli FM, Biedi C, Carbone I, Bado M, Gatti R, Minetti C. Bruno C, et al. Among authors: gandullia p. Clin Genet. 2002 Jun;61(6):465-7. doi: 10.1034/j.1399-0004.2002.610612.x. Clin Genet. 2002. PMID: 12121356 No abstract available.

6

"Syndromic diarrhea" may have better outcome than previously reported.

Barabino AV, Torrente F, Castellano E, Erba D, Calvi A, Gandullia P. Barabino AV, et al. Among authors: gandullia p. J Pediatr. 2004 Apr;144(4):553-4. doi: 10.1016/j.jpeds.2004.01.026. J Pediatr. 2004. PMID: 15069414 No abstract available.

7

[Use of computer programs in the education and self-management of patients with insulin-dependent diabetes mellitus].

Picco P, Di Rocco M, Buoncompagni A, Gandullia P, Lattere M, Borrone C. Picco P, et al. Among authors: gandullia p. Pediatr Med Chir. 1991 Sep-Oct;13(5):465-8. Pediatr Med Chir. 1991. PMID: 1788105 Italian.

8

Catheter lock and systemic infusion of linezolid for treatment of persistent Broviac catheter-related staphylococcal bacteremia.

Castagnola E, Moroni C, Gandullia P, Oddone M, Peri C, Casciaro R, De Alessandri A. Castagnola E, et al. Among authors: gandullia p. Antimicrob Agents Chemother. 2006 Mar;50(3):1120-1. doi: 10.1128/AAC.50.3.1120-1121.2006. Antimicrob Agents Chemother. 2006. PMID: 16495284 Free PMC article. No abstract available.

9

[Chronic idiopathic hypertransaminasemia].

Zancan L, Bettiol T, Rini A, Giacchino R, Gandullia P, Vajro P, Marcellini M, Musumeci S, Di Leo G, Balli F, Bragetti P, Calacoci M, Barbera C. Zancan L, et al. Among authors: gandullia p. Minerva Pediatr. 1996 May;48(5):209-16. Minerva Pediatr. 1996. PMID: 8926957 Clinical Trial. Italian.

10

Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter-->q24::q21.32-->qter) and random X inactivation.

Carrozzo R, Arrigo G, Rossi E, Bardoni B, Cammarata M, Gandullia P, Gatti R, Zuffardi O. Carrozzo R, et al. Among authors: gandullia p. Am J Med Genet. 1997 Oct 31;72(3):329-34. Am J Med Genet. 1997. PMID: 9332664

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