Bellini C - Search Results

1

Combined deficiency of xanthine oxidase and sulphite oxidase due to a deficiency of molybdenum cofactor.

Bonioli E, DiStefano A, Palmieri A, Bertola A, Bellini C, Caruso U, Fantasia AR, Minniti G, Dorche C. Bonioli E, et al. Among authors: bellini c. J Inherit Metab Dis. 1996;19(5):700-1. doi: 10.1007/BF01799850. J Inherit Metab Dis. 1996. PMID: 8892030 No abstract available.

2

Fumarate hydratase deficiency.

Bonioli E, Di Stefano A, Peri V, Caruso U, Cerone R, Lamantea E, Taroni F, Bellini C. Bonioli E, et al. Among authors: bellini c. J Inherit Metab Dis. 1998 Jun;21(4):435-6. doi: 10.1023/a:1005379330187. J Inherit Metab Dis. 1998. PMID: 9700607 No abstract available.

3

Asymptomatic intracranial hypertension associated with tetracycline use.

Bonioli E, Bellini C, Di Stefano A. Bonioli E, et al. Among authors: bellini c. Pediatr Infect Dis J. 1999 Sep;18(9):837. doi: 10.1097/00006454-199909000-00022. Pediatr Infect Dis J. 1999. PMID: 10493352 No abstract available.

4

Sebaceous nevus syndrome: report of two cases.

Bonioli EV, Bertola A, Di Stefano A, Bellini C. Bonioli EV, et al. Among authors: bellini c. Pediatr Neurol. 1997 Jul;17(1):77-9. doi: 10.1016/s0887-8994(97)80672-8. Pediatr Neurol. 1997. PMID: 9308983

5

[Follicular cysts of the mandible. The diagnostic problems].

Pesce MA, Bellini C, Di Stefano A, Bellagamba O, Palmieri A, Bonioli E. Pesce MA, et al. Among authors: bellini c. Minerva Pediatr. 1992 Mar;44(3):121-4. Minerva Pediatr. 1992. PMID: 1518493 Italian.

6

Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.

Bonioli E, Palmieri A, Bertola A, Bellini C. Bonioli E, et al. Among authors: bellini c. Genet Couns. 1995;6(4):309-12. Genet Couns. 1995. PMID: 8775417

7

Altered response to stimuli of the AP-1/DNA binding activity in a syndrome of precocious ageing (geroderma osteodysplastica hereditaria).

Gherzi R, Bellini C, Bonioli E. Gherzi R, et al. Among authors: bellini c. Mech Ageing Dev. 1998 Jan 30;100(2):169-75. doi: 10.1016/s0047-6374(97)00134-6. Mech Ageing Dev. 1998. PMID: 9541137

8

Slipped capital femoral epiphysis associated with Rubinstein-Taybi syndrome.

Bonioli E, Bellini C, Sénès FM, Palmieri A, Di Stadio M, Pinelli G. Bonioli E, et al. Among authors: bellini c. Clin Genet. 1993 Aug;44(2):79-81. doi: 10.1111/j.1399-0004.1993.tb03851.x. Clin Genet. 1993. PMID: 8275564

9

Partial agenesis of corpus callosum in LEOPARD syndrome.

Bonioli E, Di Stefano A, Costabel S, Bellini C. Bonioli E, et al. Among authors: bellini c. Int J Dermatol. 1999 Nov;38(11):855-62. doi: 10.1046/j.1365-4362.1999.00834.x. Int J Dermatol. 1999. PMID: 10583620 No abstract available.

10

Lymphodynamics in the fetus and newborn.

Bellini C, Boccardo F, Bonioli E, Campisi C. Bellini C, et al. Lymphology. 2006 Sep;39(3):110-7. Lymphology. 2006. PMID: 17036631 Review.

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