Bellini C - Search Results

1

Immunohistochemical studies in a hydroptic fetus with pulmonary lymphangiectasia and trisomy 21.

Rutigliani M, Boccardo F, Campisi C, Bonioli E, Fulcheri E, Bellini C. Rutigliani M, et al. Among authors: bellini c. Lymphology. 2007 Sep;40(3):114-21. Lymphology. 2007. PMID: 18062612

2

Rubinstein-Taybi syndrome and pheochromocytoma.

Bonioli E, Bellini C. Bonioli E, et al. Among authors: bellini c. Am J Med Genet. 1992 Oct 1;44(3):386. doi: 10.1002/ajmg.1320440325. Am J Med Genet. 1992. PMID: 1488992 No abstract available.

3

[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.

4

Therapy for hereditary nephrogenic diabetes insipidus.

Bonioli E, Bellini C. Bonioli E, et al. Among authors: bellini c. J Pediatr. 1991 Aug;119(2):331. doi: 10.1016/s0022-3476(05)80760-7. J Pediatr. 1991. PMID: 1861225 No abstract available.

5

Normal polymorphonuclear neutrophil function in a case of glycogen storage disease type Ib.

Bonioli E, Bellini C, Di Stefano A, Costa A, Canini S, Patrone F. Bonioli E, et al. Among authors: bellini c. Eur J Pediatr. 1990 Jun;149(9):665-6. doi: 10.1007/BF02034760. Eur J Pediatr. 1990. PMID: 2373123 No abstract available.

6

Inheritance of Rubinstein-Taybi syndrome.

Bonioli E, Bellini C. Bonioli E, et al. Among authors: bellini c. Am J Med Genet. 1989 Apr;32(4):559. doi: 10.1002/ajmg.1320320433. Am J Med Genet. 1989. PMID: 2774008 No abstract available.

7

Unusual association: Dandy-Walker-like malformation in the Rubinstein-Taybi syndrome.

Bonioli E, Bellini C, Di Stefano A. Bonioli E, et al. Among authors: bellini c. Am J Med Genet. 1989 Jul;33(3):420-1. doi: 10.1002/ajmg.1320330327. Am J Med Genet. 1989. PMID: 2801779 No abstract available.

8

[Facio-femoral syndrome. Description of a case with monolateral femoral hypoplasia].

Ruffa G, Bellini C, Lucigrai G, Lagorio V, Bonioli E. Ruffa G, et al. Among authors: bellini c. Minerva Pediatr. 1988 May;40(5):291-4. Minerva Pediatr. 1988. PMID: 3173281 Italian. No abstract available.

9

[Jarcho-Levin syndrome. Description of a familial case and review of the literature].

Bellini C, Scarsi M, Ruffa G, De Logu A, Bonioli E. Bellini C, et al. Minerva Pediatr. 1987 Sep 30;39(17-18):723-7. Minerva Pediatr. 1987. PMID: 3325796 Review. Italian. No abstract available.

10

[Freeman-Sheldon syndrome. Description of 2 cases of probable recessive autosomal inheritance].

Bonioli E, Bellini C, Ruffa G, Lagorio V, Gemme G. Bonioli E, et al. Among authors: bellini c. Minerva Pediatr. 1987 Feb 28;39(3-4):123-7. Minerva Pediatr. 1987. PMID: 3587189 Italian. No abstract available.

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