Cohen A - Search Results

1

Unusual presentation of Addison's disease in Schmidt's syndrome.

Gaiero A, Mulas R, Zecca S, Fichera G, Cohen A. Gaiero A, et al. Among authors: cohen a. J Pediatr Endocrinol Metab. 2003 Jun;16(5):783-5. doi: 10.1515/jpem.2003.16.5.783. J Pediatr Endocrinol Metab. 2003. PMID: 12880129

2

Distinctive characteristics of diabetes mellitus after hematopoietic cell transplantation during childhood.

Bonanomi S, Gaiero A, Masera N, Rovelli A, Uderzo C, Fichera G, Mulas R, Zecca S, Pozzi L, Cohen A. Bonanomi S, et al. Among authors: cohen a. Pediatr Transplant. 2006 Jun;10(4):461-5. doi: 10.1111/j.1399-3046.2006.00498.x. Pediatr Transplant. 2006. PMID: 16712604

3

Meier-Gorlin syndrome (ear-patella-short stature syndrome) in an Italian patient: clinical evaluation and analysis of possible candidate genes.

Cohen A, Mulas R, Seri M, Gaiero A, Fichera G, Marini M, Baffico M, Camera G. Cohen A, et al. Am J Med Genet. 2002 Jan 1;107(1):48-51. doi: 10.1002/ajmg.10083. Am J Med Genet. 2002. PMID: 11807867

4

Maxillofacial features and systemic malformations in expanded spectrum Hemifacial Microsomia.

Cohen N, Cohen E, Gaiero A, Zecca S, Fichera G, Baldi F, Giordanetto JF, Mercier JM, Cohen A. Cohen N, et al. Among authors: cohen e, cohen a. Am J Med Genet A. 2017 May;173(5):1208-1218. doi: 10.1002/ajmg.a.38151. Epub 2017 Mar 20. Am J Med Genet A. 2017. PMID: 28319315

5

Secondary thyroid carcinoma after allogeneic bone marrow transplantation during childhood.

Cohen A, Rovelli A, van Lint MT, Merlo F, Gaiero A, Mulas R, Balduzzi A, Corti P, Uderzo C, Bacigalupo A. Cohen A, et al. Bone Marrow Transplant. 2001 Dec;28(12):1125-8. doi: 10.1038/sj.bmt.1703290. Bone Marrow Transplant. 2001. PMID: 11803353

6

Endocrinological late complications after hematopoietic SCT in children.

Cohen A, Békássy AN, Gaiero A, Faraci M, Zecca S, Tichelli A, Dini G; EBMT Paediatric and Late Effects Working Parties. Cohen A, et al. Bone Marrow Transplant. 2008 Jun;41 Suppl 2:S43-8. doi: 10.1038/bmt.2008.54. Bone Marrow Transplant. 2008. PMID: 18545244 Review.

7

Salbutamol for transient tachypnea of the newborn.

Moresco L, Bruschettini M, Cohen A, Gaiero A, Calevo MG. Moresco L, et al. Among authors: cohen a. Cochrane Database Syst Rev. 2016 May 23;(5):CD011878. doi: 10.1002/14651858.CD011878.pub2. Cochrane Database Syst Rev. 2016. Update in: Cochrane Database Syst Rev. 2021 Feb 5;2:CD011878. doi: 10.1002/14651858.CD011878.pub3. PMID: 27210618 Updated. Review.

8

Central diabetes insipidus in children and young adults.

Maghnie M, Cosi G, Genovese E, Manca-Bitti ML, Cohen A, Zecca S, Tinelli C, Gallucci M, Bernasconi S, Boscherini B, Severi F, Aricò M. Maghnie M, et al. Among authors: cohen a. N Engl J Med. 2000 Oct 5;343(14):998-1007. doi: 10.1056/NEJM200010053431403. N Engl J Med. 2000. PMID: 11018166 Free article.

9

Poland sequence in two siblings suggesting an autosomal inheritance transmission.

Cohen A, Zecca S, Dassori A, Pelegrini M, Parodi L, Romano C. Cohen A, et al. Clin Genet. 1996 Aug;50(2):93-5. doi: 10.1111/j.1399-0004.1996.tb02355.x. Clin Genet. 1996. PMID: 8937768

10

A novel homozygous splicing mutation in PSAP gene causes metachromatic leukodystrophy in two Moroccan brothers.

Siri L, Rossi A, Lanza F, Mazzotti R, Costa A, Stroppiano M, Gaiero A, Cohen A, Biancheri R, Filocamo M. Siri L, et al. Among authors: cohen a. Neurogenetics. 2014 May;15(2):101-6. doi: 10.1007/s10048-014-0390-4. Epub 2014 Jan 31. Neurogenetics. 2014. PMID: 24478108

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