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Items: 9

1.

Impaired glucose metabolism in subjects with the Williams-Beuren syndrome: A five-year follow-up cohort study.

Lunati ME, Bedeschi MF, Resi V, Grancini V, Palmieri E, Salera S, Lalatta F, Pugliese G, Orsi E.

PLoS One. 2017 Oct 20;12(10):e0185371. doi: 10.1371/journal.pone.0185371. eCollection 2017.

2.

Nutritional Challenges in Duchenne Muscular Dystrophy.

Salera S, Menni F, Moggio M, Guez S, Sciacco M, Esposito S.

Nutrients. 2017 Jun 10;9(6). pii: E594. doi: 10.3390/nu9060594. Review.

3.

Birmingham epidermolysis severity score and vitamin D status are associated with low BMD in children with epidermolysis bullosa.

Rodari G, Guez S, Manzoni F, Chalouhi KK, Profka E, Bergamaschi S, Salera S, Tadini G, Ulivieri FM, Spada A, Giavoli C, Esposito S.

Osteoporos Int. 2017 Apr;28(4):1385-1392. doi: 10.1007/s00198-016-3883-1. Epub 2016 Dec 23.

PMID:
28012019
4.

Homocysteine metabolism in children and adolescents with epidermolysis bullosa.

De Giuseppe R, Venturelli G, Guez S, Salera S, De Vita C, Consonni D, Dellanoce C, Bamonti F, Chiarelli G, Manzoni F, Maiavacca R, Esposito S.

BMC Pediatr. 2016 Oct 29;16(1):173.

5.

Oral viscous budesonide as a first-line approach to esophageal stenosis in epidermolysis bullosa: an open-label trial in six children.

Zanini A, Guez S, Salera S, Farris G, Morandi A, Gentilino V, Leva E, Manzoni F, Pavesi MA, Esposito S, Macchini F.

Paediatr Drugs. 2014 Oct;16(5):391-5. doi: 10.1007/s40272-014-0086-0.

PMID:
25138121
6.

Intradialytic cycling in children and young adults on chronic hemodialysis.

Paglialonga F, Lopopolo A, Scarfia RV, Consolo S, Galli MA, Salera S, Grassi MR, Brivio A, Edefonti A.

Pediatr Nephrol. 2014 Mar;29(3):431-8. doi: 10.1007/s00467-013-2675-5. Epub 2013 Nov 21.

PMID:
24253591
7.

Correlates of exercise capacity in pediatric patients on chronic hemodialysis.

Paglialonga F, Lopopolo A, Scarfia RV, Galli MA, Consolo S, Brivio A, Grassi MR, Salera S, Edefonti A.

J Ren Nutr. 2013 Sep;23(5):380-6. doi: 10.1053/j.jrn.2013.04.006. Epub 2013 Jun 22.

PMID:
23800461
8.

Severe vitamin B12 deficiency in an exclusively breastfed 5-month-old Italian infant born to a mother receiving multivitamin supplementation during pregnancy.

Guez S, Chiarelli G, Menni F, Salera S, Principi N, Esposito S.

BMC Pediatr. 2012 Jun 24;12:85. doi: 10.1186/1471-2431-12-85.

9.

Medium-chain triglyceride loading test in carnitine-acylcarnitine translocase deficiency: insights on treatment.

Parini R, Invernizzi F, Menni F, Garavaglia B, Melotti D, Rimoldi M, Salera S, Tosetto C, Taroni F.

J Inherit Metab Dis. 1999 Aug;22(6):733-9.

PMID:
10472533

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