D'Ambrosio A - Search Results

1

Germ-line mutation of the NRAS gene may be responsible for the development of juvenile myelomonocytic leukaemia.

De Filippi P, Zecca M, Lisini D, Rosti V, Cagioni C, Carlo-Stella C, Radi O, Veggiotti P, Mastronuzzi A, Acquaviva A, D'Ambrosio A, Locatelli F, Danesino C. De Filippi P, et al. Br J Haematol. 2009 Dec;147(5):706-9. doi: 10.1111/j.1365-2141.2009.07894.x. Epub 2009 Sep 22. Br J Haematol. 2009. PMID: 19775298 Free article.

2

Celiac disease in a patient with beta-thalassemia major.

Acquaviva A, Municchi G, Marconcini S, D'Ambrosio A, Morgese G. Acquaviva A, et al. J Pediatr Gastroenterol Nutr. 2003 Apr;36(4):489-91. doi: 10.1097/00005176-200304000-00014. J Pediatr Gastroenterol Nutr. 2003. PMID: 12658042 No abstract available.

3

Hypereosinophilic syndrome in childhood: clinical and molecular features of two cases.

Farruggia P, D'Angelo P, Acquaviva A, Trizzino A, Tucci F, Cilloni D, Messa F, D'Ambrosio A, Aricò M. Farruggia P, et al. Pediatr Hematol Oncol. 2009 Apr-May;26(3):129-35. doi: 10.1080/08880010902773024. Pediatr Hematol Oncol. 2009. PMID: 19382034

4

Central precocious puberty in multisystem Langerhans cell histiocytosis: a case report.

Municchi G, Marconcini S, D'Ambrosio A, Berardi R, Acquaviva A. Municchi G, et al. Pediatr Hematol Oncol. 2002 Jun;19(4):273-8. doi: 10.1080/08880010252899451. Pediatr Hematol Oncol. 2002. PMID: 12051595

5

Vagal and hypoglossal Bell's palsy.

Zannolli R, Acquaviva A, D'Ambrosio A, Pucci L, Balestri P, Morgese G. Zannolli R, et al. J Child Neurol. 2000 Feb;15(2):130-2. doi: 10.1177/088307380001500213. J Child Neurol. 2000. PMID: 10695899

6

[Idiopathic pulmonary hemosiderosis].

Capaccioli L, D'Ambrosio A, Paciotti F, Acquaviva A, Morgese G. Capaccioli L, et al. Pediatria (Napoli). 1978 Sep 30;86(3):471-8. Pediatria (Napoli). 1978. PMID: 754167 Italian. No abstract available.

7

Medical therapy of retinoblastoma in children.

Acquaviva A, Barberi L, Bernardini C, D'Ambrosio A, Lasorella G. Acquaviva A, et al. J Neurosurg Sci. 1982 Jan-Mar;26(1):49-52. J Neurosurg Sci. 1982. PMID: 7143085

8

Medical therapy of orbit rhabdomyosarcoma in children.

Acquaviva A, Barberi L, Bernardini C, D'Ambrosio A, Lasorella G. Acquaviva A, et al. J Neurosurg Sci. 1982 Jan-Mar;26(1):45-8. J Neurosurg Sci. 1982. PMID: 7143084

9

Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degeneration.

Zannolli R, Gilman S, Rossi S, Volpi N, Bernini A, Galluzzi P, Galimberti D, Pucci L, D'Ambrosio A, Morgese G, Giannini F. Zannolli R, et al. Arch Neurol. 2002 Aug;59(8):1319-26. doi: 10.1001/archneur.59.8.1319. Arch Neurol. 2002. PMID: 12164731

10

Abnormalities of the thyroid in survivors of childhood Hodgkin's disease.

Rodriquez DC, Guidoni E, D'ambrosio A, Pochiero F, Caini M, Guglielmucci D, Lucherini M, Carra F, Municchi G. Rodriquez DC, et al. Minerva Pediatr. 2014 Aug;66(4):249-56. Minerva Pediatr. 2014. PMID: 25198559

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