Di Pasquale G - Search Results

1

Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes.

Balsamo A, Wasniewska M, Di Pasquale G, Salzano G, Baronio F, Bombaci S, De Luca F. Balsamo A, et al. Among authors: di pasquale g. Eur J Pediatr. 2006 Jun;165(6):380-3. doi: 10.1007/s00431-005-0075-y. Epub 2006 Mar 7. Eur J Pediatr. 2006. PMID: 16520942

2

In Sicilian ethnic group non-classical congenital adrenal hyperplasia is frequently associated with a very mild genotype.

Wasniewska M, Di Pasquale G, Rulli I, Salzano G, Caruso M, Indovina S, Di Pasquale L, Zirilli G, De Luca F. Wasniewska M, et al. Among authors: di pasquale l, di pasquale g. J Endocrinol Invest. 2007 Mar;30(3):181-5. doi: 10.1007/BF03347422. J Endocrinol Invest. 2007. PMID: 17505149

3

Transient electrocardiographic changes suggesting myocardial ischaemia in newborn infants following tocolysis with beta-sympathomimetics.

Gemelli M, De Luca F, Manganaro R, Leonardi R, Rando F, Agnetti A, Mami C, Di Pasquale G. Gemelli M, et al. Among authors: di pasquale g. Eur J Pediatr. 1990 Jul;149(10):730-3. doi: 10.1007/BF01959533. Eur J Pediatr. 1990. PMID: 1976519

4

Salt wasting phenotype in a compound heterozygous girl with P482S mutation associated with anovel mutation of CYP21 gene (Q481P).

Di Pasquale G, Wasniewska M, Caruso M, Salzano G, Coco M, Lombardo F, De Luca F. Di Pasquale G, et al. J Endocrinol Invest. 2005 Dec;28(11):1038-9. doi: 10.1007/BF03345346. J Endocrinol Invest. 2005. PMID: 16483186 No abstract available.

5

Thyroid function in children with cystic fibrosis.

De Luca F, Trimarchi F, Sferlazzas C, Benvenga S, Costante G, Mami C, Di Pasquale G, Magazzu G. De Luca F, et al. Among authors: di pasquale g. Eur J Pediatr. 1982 Jul;138(4):327-30. doi: 10.1007/BF00442510. Eur J Pediatr. 1982. PMID: 6813123

6

Long-term results with growth hormone therapy in idiopathic hypopituitarism.

Bernasconi S, Arrigo T, Wasniewsk M, Ghizzoni L, Ruggeri C, Di Pasquale G, Vottero A, De Luca F. Bernasconi S, et al. Among authors: di pasquale g. Horm Res. 2000;53 Suppl 1:55-9. doi: 10.1159/000053206. Horm Res. 2000. PMID: 10895044 Review.

7

TTF-2/FOXE1 gene polymorphisms in Sicilian patients with permanent primary congenital hypothyroidism.

Santarpia L, Valenzise M, Di Pasquale G, Arrigo T, San Martino G, Cicciò MP, Trimarchi F, De Luca F, Benvenga S. Santarpia L, et al. Among authors: di pasquale g. J Endocrinol Invest. 2007 Jan;30(1):13-9. doi: 10.1007/BF03347390. J Endocrinol Invest. 2007. PMID: 17318017

8

Involvement of fractalkine and macrophage inflammatory protein-1 alpha in moderate-severe depression.

Merendino RA, Di Pasquale G, De Luca F, Di Pasquale L, Ferlazzo E, Martino G, Palumbo MC, Morabito F, Gangemi S. Merendino RA, et al. Among authors: di pasquale l, di pasquale g. Mediators Inflamm. 2004 Jun;13(3):205-7. doi: 10.1080/09511920410001713484. Mediators Inflamm. 2004. PMID: 15223613 Free PMC article.

9

Temporal trends in the epidemiology, management, and outcome of patients with cardiogenic shock complicating acute coronary syndromes.

De Luca L, Olivari Z, Farina A, Gonzini L, Lucci D, Di Chiara A, Casella G, Chiarella F, Boccanelli A, Di Pasquale G, De Servi S, Bovenzi FM, Gulizia MM, Savonitto S. De Luca L, et al. Among authors: di chiara a, di pasquale g. Eur J Heart Fail. 2015 Nov;17(11):1124-32. doi: 10.1002/ejhf.339. Epub 2015 Sep 4. Eur J Heart Fail. 2015. PMID: 26339723 Free article.

10

Trends in management and outcome of patients with non-ST elevation acute coronary syndromes and peripheral arterial disease.

De Luca L, Di Pasquale G, Gonzini L, Chiarella F, Di Chiara A, Boccanelli A, Casella G, Olivari Z, De Servi S, Gulizia MM, Di Lenarda A, Savonitto S, Bolognese L. De Luca L, et al. Among authors: di chiara a, di lenarda a, di pasquale g. Eur J Intern Med. 2019 Jan;59:70-76. doi: 10.1016/j.ejim.2018.08.010. Epub 2018 Aug 25. Eur J Intern Med. 2019. PMID: 30154039

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