Zampino G - Search Results

1

Cystic Hygroma: A Preliminary Genetic Study and a Short Review from the Literature.

Noia G, Maltese PE, Zampino G, D'Errico M, Cammalleri V, Convertini P, Marceddu G, Mueller M, Guerri G, Bertelli M. Noia G, et al. Among authors: zampino g. Lymphat Res Biol. 2019 Feb;17(1):30-39. doi: 10.1089/lrb.2017.0084. Epub 2018 Nov 22. Lymphat Res Biol. 2019. PMID: 30475086 Review.

2

Constitutional trisomy 8 and myelodysplasia: report of a case and review of the literature.

Zollino M, Genuardi M, Bajer J, Tornesello A, Mastrangelo S, Zampino G, Mastrangelo R, Neri G. Zollino M, et al. Among authors: zampino g. Leuk Res. 1995 Oct;19(10):733-6. doi: 10.1016/0145-2126(95)00050-x. Leuk Res. 1995. PMID: 7500650

3

Second case of hepatoblastoma in a young patient with Simpson-Golabi-Behmel syndrome.

Buonuomo PS, Ruggiero A, Vasta I, Attinà G, Riccardi R, Zampino G. Buonuomo PS, et al. Among authors: zampino g. Pediatr Hematol Oncol. 2005 Oct-Nov;22(7):623-8. doi: 10.1080/08880010500198988. Pediatr Hematol Oncol. 2005. PMID: 16166055

4

A newborn with multiple fractures as first presentation of infantile myofibromatosis.

Buonuomo PS, Ruggiero A, Zampino G, Maurizi P, Attinà G, Riccardi R. Buonuomo PS, et al. Among authors: zampino g. J Perinatol. 2006 Oct;26(10):653-5. doi: 10.1038/sj.jp.7211581. J Perinatol. 2006. PMID: 17006529

5

Melanocytic nevi in RASopathies: insights on dermatological diagnostic handles.

Leoni C, Guerriero C, Onesimo R, Coco V, Di Ruscio C, Acampora A, Esposito I, Romano A, Tartaglia M, Genuardi M, Zampino G. Leoni C, et al. Among authors: zampino g. J Eur Acad Dermatol Venereol. 2021 Jan;35(1):e83-e85. doi: 10.1111/jdv.16824. Epub 2020 Aug 4. J Eur Acad Dermatol Venereol. 2021. PMID: 32679607 No abstract available.

6

New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and pachygyria.

Zollino M, Mastroiacovo P, Zampino G, Mariotti P, Neri G. Zollino M, et al. Among authors: zampino g. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):452-7. doi: 10.1002/ajmg.1320430168. Am J Med Genet. 1992. PMID: 1605225

7

Further contribution to the description of phenotypes associated with partial 4q duplication.

Zollino M, Zampino G, Torrioli G, Pomponi MG, Neri G. Zollino M, et al. Among authors: zampino g. Am J Med Genet. 1995 May 22;57(1):69-73. doi: 10.1002/ajmg.1320570116. Am J Med Genet. 1995. PMID: 7645603 Review.

8

Costello syndrome: further clinical delineation, natural history, genetic definition, and nosology.

Zampino G, Mastroiacovo P, Ricci R, Zollino M, Segni G, Martini-Neri ME, Neri G. Zampino G, et al. Am J Med Genet. 1993 Aug 15;47(2):176-83. doi: 10.1002/ajmg.1320470210. Am J Med Genet. 1993. PMID: 8213903 Review.

9

Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome.

Zollino M, Di Stefano C, Zampino G, Mastroiacovo P, Wright TJ, Sorge G, Selicorni A, Tenconi R, Zappalà A, Battaglia A, Di Rocco M, Palka G, Pallotta R, Altherr MR, Neri G. Zollino M, et al. Among authors: zampino g. Am J Med Genet. 2000 Sep 18;94(3):254-61. doi: 10.1002/1096-8628(20000918)94:3<254::aid-ajmg13>3.0.co;2-7. Am J Med Genet. 2000. PMID: 10995514

10

Diamond-Blackfan anemia and midline defects.

Ruggiero A, Zampino G, Mastroiacovo P, Riccardi R. Ruggiero A, et al. Among authors: zampino g. J Pediatr Hematol Oncol. 2000 Sep-Oct;22(5):479-80. doi: 10.1097/00043426-200009000-00021. J Pediatr Hematol Oncol. 2000. PMID: 11037867 No abstract available.

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