Giuffrè L - Search Results

1

Cammarata M, Corsello G, Marino M, Morabito M, Pecoraro MR, Piccione M, Giuffrè L. Cammarata M, et al. Among authors: giuffre l. Acta Eur Fertil. 1989 Nov-Dec;20(6):367-70. Acta Eur Fertil. 1989. PMID: 2488982

2

Holoprosencephaly: examples of clinical variability and etiologic heterogeneity.

Corsello G, Buttitta P, Cammarata M, Lo Presti A, Maresi E, Zumpani L, Giuffrè L. Corsello G, et al. Among authors: giuffre l. Am J Med Genet. 1990 Oct;37(2):244-9. doi: 10.1002/ajmg.1320370216. Am J Med Genet. 1990. PMID: 2147361

3

Two new cases of thrombocytopenia absent radius (TAR) syndrome: clinical, genetic and nosologic features.

Giuffrè L, Cammarata M, Corsello G, Vitaliti SM. Giuffrè L, et al. Klin Padiatr. 1988 Jan-Feb;200(1):10-4. doi: 10.1055/s-2008-1033677. Klin Padiatr. 1988. PMID: 3367608

4

[Role of diagnostic imaging in Rubinstein-Taybi syndrome. Personal experience with 8 cases].

Albanese A, Giuffrè L, Carcione A, Corsello G, Benenati A, Cammarata M, Albano S, Piccione M, Rubino FP, Reina C, et al. Albanese A, et al. Among authors: giuffre l. Radiol Med. 1991 Mar;81(3):253-61. Radiol Med. 1991. PMID: 2014329 Italian.

5

Growth charts of Down syndrome in Sicily: evaluation of 382 children 0-14 years of age.

Piro E, Pennino C, Cammarata M, Corsello G, Grenci A, Lo Giudice C, Morabito M, Piccione M, Giuffrè L. Piro E, et al. Among authors: giuffre l. Am J Med Genet Suppl. 1990;7:66-70. doi: 10.1002/ajmg.1320370712. Am J Med Genet Suppl. 1990. PMID: 2149977

6

[Ring chromosome 4 in twins].

Giuffrè L, Cammarata M, Corsello G, Benigno V, Graziano L, Roccella F, Balsamo V. Giuffrè L, et al. Pediatr Med Chir. 1987 May-Jun;9(3):349-50. Pediatr Med Chir. 1987. PMID: 3671134 Italian.

7

New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.

Giuffrè L, Corsello G, Giuffrè M, Piccione M, Albanese A. Giuffrè L, et al. Among authors: giuffre m. Am J Med Genet. 1994 Jul 1;51(3):266-9. doi: 10.1002/ajmg.1320510319. Am J Med Genet. 1994. PMID: 8074157

8

VATER/VACTERL association: clinical variability and expanding phenotype including laryngeal stenosis.

Corsello G, Maresi E, Corrao AM, Dimita U, Lo Cascio M, Cammarata M, Giuffrè L. Corsello G, et al. Among authors: giuffre l. Am J Med Genet. 1992 Dec 1;44(6):813-5. doi: 10.1002/ajmg.1320440619. Am J Med Genet. 1992. PMID: 1481853

9

Cervico-oculo-acusticus (Wildervanck's) syndrome: a clinical variant of Klippel-Feil sequence?

Corsello G, Carcione A, Castro L, Giuffrè L. Corsello G, et al. Among authors: giuffre l. Klin Padiatr. 1990 May-Jun;202(3):176-9. doi: 10.1055/s-2007-1025514. Klin Padiatr. 1990. PMID: 2355722

10

[Male pseudohermaphroditism related to 17-alpha hydroxylase deficiency].

Liotta A, Cammarata M, Corsello G, Ferrara D, Giuffrè L. Liotta A, et al. Among authors: giuffre l. Pediatr Med Chir. 1987 May-Jun;9(3):309-10. Pediatr Med Chir. 1987. PMID: 2823235 Italian.

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