Cappa M - Search Results

1

Clinical and roentgenographic findings in a patient with primordial microcephalic dwarfism type Caroline Crachami.

Boscherini B, Colabucci F, Galasso C, Marietti G, Cappa M, Pasquino AM. Boscherini B, et al. Among authors: cappa m. Am J Med Genet. 1996 Dec 18;66(3):269-72. doi: 10.1002/(SICI)1096-8628(19961218)66:3<269::AID-AJMG6>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8985485

2

Precocious puberty with hypothalamic hamartoma and non classical form of congenital adrenal hyperplasia. Report of two cases.

Pasquino AM, Pucarelli I, Cambiaso P, Cappa M. Pasquino AM, et al. Among authors: cappa m. Minerva Pediatr. 2009 Oct;61(5):561-4. Minerva Pediatr. 2009. PMID: 19794382

3

Is IGF binding protein-3 assessment helpful for the diagnosis of GH deficiency?

Cianfarani S, Boemi S, Spagnoli A, Cappa M, Argirò G, Vaccaro F, Manca Bitti ML, Boscherini B. Cianfarani S, et al. Among authors: cappa m. Clin Endocrinol (Oxf). 1995 Jul;43(1):43-7. doi: 10.1111/j.1365-2265.1995.tb01891.x. Clin Endocrinol (Oxf). 1995. PMID: 7543832

4

Early retesting by GHRH + arginine test shows normal GH response in most children with idiopathic GH deficiency.

Bizzarri C, Pedicelli S, Boscherini B, Bedogni G, Cappa M, Cianfarani S. Bizzarri C, et al. Among authors: cappa m. J Endocrinol Invest. 2015 Apr;38(4):429-36. doi: 10.1007/s40618-014-0205-3. Epub 2014 Nov 7. J Endocrinol Invest. 2015. PMID: 25376365

5

[The empty sella in children. Clinical, diagnostic and therapeutic aspects].

Di Rocco C, Iannelli A, Maira G, Colabucci F, Borrelli P, Cappa M. Di Rocco C, et al. Among authors: cappa m. Minerva Pediatr. 1984 Aug 31;36(15-16):745-53. Minerva Pediatr. 1984. PMID: 6513903 Italian. No abstract available.

6

Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria.

Zollino M, Battaglia A, D'Avanzo MG, Della Bruna MM, Marini R, Scarano G, Cappa M, Neri G. Zollino M, et al. Among authors: cappa m. Am J Med Genet. 1994 Sep 1;52(3):302-7. doi: 10.1002/ajmg.1320520310. Am J Med Genet. 1994. PMID: 7810561

7

Auxological evaluation in patients with DiGeorge/velocardiofacial syndrome (deletion 22q11.2 syndrome).

Digilio MC, Marino B, Cappa M, Cambiaso P, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: cappa m. Genet Med. 2001 Jan-Feb;3(1):30-3. doi: 10.1097/00125817-200101000-00007. Genet Med. 2001. PMID: 11339374 Free article.

8

XK-aprosencephaly and related entities.

Renzetti G, Villani A, Bizzarri C, Chessa L, Vignati E, Gianotti A, Cappa M, Szakacs J, Townsend JJ, Miller ME, Opitz JM, Kennedy AM, Byrne JL. Renzetti G, et al. Among authors: cappa m. Am J Med Genet A. 2005 Nov 1;138(4):401-10. doi: 10.1002/ajmg.a.30600. Am J Med Genet A. 2005. PMID: 16208689 Review.

9

McCune-Albright syndrome: a longitudinal clinical study of 32 patients.

de Sanctis C, Lala R, Matarazzo P, Balsamo A, Bergamaschi R, Cappa M, Cisternino M, de Sanctis V, Lucci M, Franzese A, Ghizzoni L, Pasquino AM, Segni M, Rigon F, Saggese G, Bertelloni S, Buzi F. de Sanctis C, et al. Among authors: cappa m. J Pediatr Endocrinol Metab. 1999 Nov-Dec;12(6):817-26. doi: 10.1515/jpem.1999.12.6.817. J Pediatr Endocrinol Metab. 1999. PMID: 10614538 Review.

10

Nonsyndromal overgrowth in males with mild psychomotor delay.

Neri G, Steindl K, Mazzei A, Battaglia A, Cappa M. Neri G, et al. Among authors: cappa m. Am J Med Genet. 1998 Oct 2;79(4):291-3. Am J Med Genet. 1998. PMID: 9781910

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