Starling A - Search Results

1

Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum.

de Paula F, Vieira N, Starling A, Yamamoto LU, Lima B, de Cássia Pavanello R, Vainzof M, Nigro V, Zatz M. de Paula F, et al. Among authors: starling a. Eur J Hum Genet. 2003 Dec;11(12):923-30. doi: 10.1038/sj.ejhg.5201066. Eur J Hum Genet. 2003. PMID: 14647208

2

A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.

Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M. Starling A, et al. Eur J Hum Genet. 2004 Dec;12(12):1033-40. doi: 10.1038/sj.ejhg.5201289. Eur J Hum Genet. 2004. PMID: 15367920

3

The 10 autosomal recessive limb-girdle muscular dystrophies.

Zatz M, de Paula F, Starling A, Vainzof M. Zatz M, et al. Among authors: starling a. Neuromuscul Disord. 2003 Sep;13(7-8):532-44. doi: 10.1016/s0960-8966(03)00100-7. Neuromuscul Disord. 2003. PMID: 12921790 Review.

4

Calpainopathy: how broad is the spectrum of clinical variability?

Starling A, de Paula F, Silva H, Vainzof M, Zatz M. Starling A, et al. J Mol Neurosci. 2003;21(3):233-6. doi: 10.1385/jmn:21:3:233. J Mol Neurosci. 2003. PMID: 14645990

5

A family with McLeod syndrome and calpainopathy with clinically overlapping diseases.

Starling A, Schlesinger D, Kok F, Passos-Bueno MR, Vainzof M, Zatz M. Starling A, et al. Neurology. 2005 Dec 13;65(11):1832-3. doi: 10.1212/01.wnl.0000187073.58307.41. Neurology. 2005. PMID: 16344536

6

Calpains and disease.

Zatz M, Starling A. Zatz M, et al. Among authors: starling a. N Engl J Med. 2005 Jun 9;352(23):2413-23. doi: 10.1056/NEJMra043361. N Engl J Med. 2005. PMID: 15944426 Review. No abstract available.

7

A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large Brazilian pedigree.

Mitne-Neto M, Kok F, Beetz C, Pessoa A, Bueno C, Graciani Z, Martyn M, Monteiro CB, Mitne G, Hubert P, Nygren AO, Valadares M, Cerqueira AM, Starling A, Deufel T, Zatz M. Mitne-Neto M, et al. Among authors: starling a. Eur J Hum Genet. 2007 Dec;15(12):1276-9. doi: 10.1038/sj.ejhg.5201924. Epub 2007 Sep 26. Eur J Hum Genet. 2007. PMID: 17895902

8

Further evidence for a fourth gene causing X-linked pure spastic paraplegia.

Starling A, Rocco P, Cambi F, Hobson GM, Passos Bueno MR, Zatz M. Starling A, et al. Am J Med Genet. 2002 Aug 1;111(2):152-6. doi: 10.1002/ajmg.10551. Am J Med Genet. 2002. PMID: 12210342

9

Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13.

Macedo-Souza LI, Kok F, Santos S, Amorim SC, Starling A, Nishimura A, Lezirovitz K, Lino AM, Zatz M. Macedo-Souza LI, et al. Among authors: starling a. Ann Neurol. 2005 May;57(5):730-7. doi: 10.1002/ana.20478. Ann Neurol. 2005. PMID: 15852396

10

Autosomal dominant (AD) pure spastic paraplegia (HSP) linked to locus SPG4 affects almost exclusively males in a large pedigree.

Starling A, Rocco P, Passos-Bueno MR, Hazan J, Marie SK, Zatz M. Starling A, et al. J Med Genet. 2002 Dec;39(12):e77. doi: 10.1136/jmg.39.12.e77. J Med Genet. 2002. PMID: 12471215 Free PMC article. No abstract available.

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