Migone N - Search Results

1

Genotype, phenotype and hormonal levels correlation in non-classical congenital adrenal hyperplasia.

Einaudi S, Napolitano E, Restivo F, Motta G, Baldi M, Tuli G, Grosso E, Migone N, Menegatti E, Manieri C. Einaudi S, et al. Among authors: migone n. J Endocrinol Invest. 2011 Oct;34(9):660-4. doi: 10.3275/7410. Epub 2010 Dec 15. J Endocrinol Invest. 2011. PMID: 21169730

2

TSC1 and TSC2 deletions differ in size, preference for recombinatorial sequences, and location within the gene.

Longa L, Saluto A, Brusco A, Polidoro S, Padovan S, Allavena A, Carbonara C, Grosso E, Migone N. Longa L, et al. Among authors: migone n. Hum Genet. 2001 Feb;108(2):156-66. doi: 10.1007/s004390100460. Hum Genet. 2001. PMID: 11281455

3

New understandings of the genetic basis of isolated idiopathic central hypogonadism.

Bonomi M, Libri DV, Guizzardi F, Guarducci E, Maiolo E, Pignatti E, Asci R, Persani L; Idiopathic Central Hypogonadism Study Group of the Italian Societies of Endocrinology and Pediatric Endocrinology and Diabetes. Bonomi M, et al. Asian J Androl. 2012 Jan;14(1):49-56. doi: 10.1038/aja.2011.68. Epub 2011 Dec 5. Asian J Androl. 2012. PMID: 22138902 Free PMC article. Review.

4

Molecular genetic analysis of von Hippel-Lindau disease by denaturing high-performance liquid chromatography.

Menegatti E, Ferrone M, Gallone S, Mameli M, Grosso E, Migone N. Menegatti E, et al. Among authors: migone n. Contrib Nephrol. 2001;(136):306-11. doi: 10.1159/000060206. Contrib Nephrol. 2001. PMID: 11688398 No abstract available.

5

Maternal serum markers. Estimation of the risk of Down's syndrome: a prospective study.

Mancini G, Perona M, Dall'Amico D, Bollati C, Albano F, Mazzone R, Rosso M, Grosso E, Migone N, Fiocchi F, et al. Mancini G, et al. Among authors: migone n. Int J Clin Lab Res. 1994;24(1):49-53. doi: 10.1007/BF02592410. Int J Clin Lab Res. 1994. PMID: 7514056

6

Bilaterally cleft lip and bilateral thumb polydactyly with triphalangeal component in a patient with two de novo deletions of HSA 4q32 and 4q34 involving PDGFC, GRIA2, and FBXO8 genes.

Calcia A, Gai G, Di Gregorio E, Talarico F, Naretto VG, Migone N, Pepe E, Grosso E, Brusco A. Calcia A, et al. Among authors: migone n. Am J Med Genet A. 2013 Oct;161A(10):2656-62. doi: 10.1002/ajmg.a.36146. Epub 2013 Aug 16. Am J Med Genet A. 2013. PMID: 24038848 Review.

7

The polymorphic polyglutamine repeat in the mitochondrial DNA polymerase gamma gene is not associated with oligozoospermia.

Brusco A, Michielotto C, Gatta V, Foresta C, Matullo G, Zeviani M, Ferrari G, Dragone E, Calabrese G, Rossato M, Stuppia L, Migone N. Brusco A, et al. Among authors: migone n. J Endocrinol Invest. 2006 Jan;29(1):1-4. doi: 10.1007/BF03349169. J Endocrinol Invest. 2006. PMID: 16553026

8

A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations.

Brussino A, Vaula G, Cagnoli C, Panza E, Seri M, Di Gregorio E, Scappaticci S, Camanini S, Daniele D, Bradac GB, Pinessi L, Cavalieri S, Grosso E, Migone N, Brusco A. Brussino A, et al. Among authors: migone n. Eur J Neurol. 2010 Apr;17(4):541-9. doi: 10.1111/j.1468-1331.2009.02844.x. Epub 2009 Dec 4. Eur J Neurol. 2010. PMID: 19961535

9

9q34 loss of heterozygosity in a tuberous sclerosis astrocytoma suggests a growth suppressor-like activity also for the TSC1 gene.

Carbonara C, Longa L, Grosso E, Borrone C, Garrè MG, Brisigotti M, Migone N. Carbonara C, et al. Among authors: migone n. Hum Mol Genet. 1994 Oct;3(10):1829-32. doi: 10.1093/hmg/3.10.1829. Hum Mol Genet. 1994. PMID: 7849708

10

A late onset variant of ataxia-telangiectasia with a compound heterozygous genotype, A8030G/7481insA.

Saviozzi S, Saluto A, Taylor AM, Last JI, Trebini F, Paradiso MC, Grosso E, Funaro A, Ponzio G, Migone N, Brusco A. Saviozzi S, et al. Among authors: migone n. J Med Genet. 2002 Jan;39(1):57-61. doi: 10.1136/jmg.39.1.57. J Med Genet. 2002. PMID: 11826028 Free PMC article. No abstract available.

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