Baldinotti F - Search Results

1

Premature ovarian failure and fragile X premutation: a study on 45 women.

Bussani C, Papi L, Sestini R, Baldinotti F, Bucciantini S, Bruni V, Scarselli G. Bussani C, et al. Among authors: baldinotti f. Eur J Obstet Gynecol Reprod Biol. 2004 Feb 10;112(2):189-91. doi: 10.1016/j.ejogrb.2003.06.003. Eur J Obstet Gynecol Reprod Biol. 2004. PMID: 14746957

2

Clinical characteristics and genetic analysis in women with premature ovarian insufficiency.

Ferrarini E, Russo L, Fruzzetti F, Agretti P, De Marco G, Dimida A, Gianetti E, Simoncini T, Simi P, Baldinotti F, Benelli E, Pucci E, Pinchera A, Vitti P, Tonacchera M. Ferrarini E, et al. Among authors: baldinotti f. Maturitas. 2013 Jan;74(1):61-7. doi: 10.1016/j.maturitas.2012.09.017. Epub 2012 Oct 26. Maturitas. 2013. PMID: 23107817

3

Cx26 gene mutations in idiopathic progressive hearing loss.

Ravecca F, Berrettini S, Forli F, Marcaccini M, Casani A, Baldinotti F, Fogli A, Siciliano G, Simi P. Ravecca F, et al. Among authors: baldinotti f. J Otolaryngol. 2005 Apr;34(2):126-34. doi: 10.2310/7070.2005.04017. J Otolaryngol. 2005. PMID: 16076412

4

Nonsense mutation in exon 2 of the alpha-galactosidase A gene in a patient with Fabry disease.

Manni E, Fogli A, Baldinotti F, Rossi S, Funel N, Barachini P, Simi P. Manni E, et al. Among authors: baldinotti f. Contrib Nephrol. 2001;(136):223-8. doi: 10.1159/000060192. Contrib Nephrol. 2001. PMID: 11688384 No abstract available.

5

Regulation of telomerase and its hTERT messenger in colorectal cancer.

Boldrini L, Faviana P, Gisfredi S, Donati V, Zucconi Y, Ursino S, Simi P, Baldinotti F, Berti P, Galleri D, Materazzi G, Basolo F, Miccoli P, Pingitore R, Fontanini G. Boldrini L, et al. Among authors: baldinotti f. Oncol Rep. 2004 Feb;11(2):395-400. Oncol Rep. 2004. PMID: 14719074

6

Female phenotype at birth and postnatal masculinization, during the first months of life, associated with transient 5 alpha-reductase 2 deficiency in a preterm infant. A timing defect syndrome?

Vuerich M, Ghirri P, Merusi I, Cuttano A, Baldinotti F, Simi P, Migeon CJ, Boldrini A. Vuerich M, et al. Among authors: baldinotti f. Minerva Pediatr. 2003 Oct;55(5 Suppl 1):82. Minerva Pediatr. 2003. PMID: 14992191 No abstract available.

7

Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic man.

Valetto A, Bertini V, Rapalini E, Baldinotti F, Di Martino D, Simi P. Valetto A, et al. Among authors: baldinotti f. Fertil Steril. 2004 May;81(5):1388-90. doi: 10.1016/j.fertnstert.2003.09.069. Fertil Steril. 2004. PMID: 15136108 Free article.

8

Novel human pathological mutations. Gene symbol: SPG4. Disease: spastic paraplegia, autosomal dominant.

Fogli A, Battini R, Baldinotti F, Conidi ME, Michelucci A, Simi P. Fogli A, et al. Among authors: baldinotti f. Hum Genet. 2009 Aug;126(2):340. Hum Genet. 2009. PMID: 19694022 No abstract available.

9

Body composition and metabolic profile in women with complete androgen insensitivity syndrome.

Dati E, Baroncelli GI, Mora S, Russo G, Baldinotti F, Parrini D, Erba P, Simi P, Bertelloni S. Dati E, et al. Among authors: baldinotti f. Sex Dev. 2009;3(4):188-93. doi: 10.1159/000228719. Epub 2009 Sep 11. Sex Dev. 2009. PMID: 19752598

10

A girl with tomboy behavior: lesson from misdiagnosis in a baby with ambiguous genitalia.

Dati E, Baldinotti F, Conidi ME, Simi P, Baroncelli GI, Bertelloni S. Dati E, et al. Among authors: baldinotti f. Sex Dev. 2010;4(3):150-4. doi: 10.1159/000273265. Epub 2009 Dec 30. Sex Dev. 2010. PMID: 20051677

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