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621 results

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Page 1
Pediatric multiple sclerosis report of 14 cases.
Guilhoto LM, Osório CA, Machado LR, de Castro CP, Manreza ML, Callegaro D, Kok F, Diament A. Guilhoto LM, et al. Among authors: kok f. Brain Dev. 1995 Jan-Feb;17(1):9-12. doi: 10.1016/0387-7604(94)00091-b. Brain Dev. 1995. PMID: 7762771
A clinical study of 77 patients with mucopolysaccharidosis type II.
Schwartz IV, Ribeiro MG, Mota JG, Toralles MB, Correia P, Horovitz D, Santos ES, Monlleo IL, Fett-Conte AC, Sobrinho RP, Norato DY, Paula AC, Kim CA, Duarte AR, Boy R, Valadares E, De Michelena M, Mabe P, Martinhago CD, Pina-Neto JM, Kok F, Leistner-Segal S, Burin MG, Giugliani R. Schwartz IV, et al. Among authors: kok f. Acta Paediatr. 2007 Apr;96(455):63-70. doi: 10.1111/j.1651-2227.2007.00212.x. Acta Paediatr. 2007. PMID: 17391446
Clinical and biochemical study of 29 Brazilian patients with metachromatic leukodystrophy.
Artigalás O, Lagranha VL, Saraiva-Pereira ML, Burin MG, Lourenço CM, van der Linden H Jr, Santos ML, Rosemberg S, Steiner CE, Kok F, de Souza CF, Jardim LB, Giugliani R, Schwartz IV. Artigalás O, et al. Among authors: kok f. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S257-62. doi: 10.1007/s10545-010-9140-4. Epub 2010 Jul 2. J Inherit Metab Dis. 2010. PMID: 20596894
Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS.
Rezende Filho FM, Parkinson MH, Pedroso JL, Poh R, Faber I, Lourenço CM, Júnior WM, França Junior MC, Kok F, Sallum JMF, Giunti P, Barsottini OGP. Rezende Filho FM, et al. Among authors: kok f. Parkinsonism Relat Disord. 2019 May;62:148-155. doi: 10.1016/j.parkreldis.2018.12.024. Epub 2018 Dec 23. Parkinsonism Relat Disord. 2019. PMID: 30638817
Friedreich's ataxia: clinical and molecular study of 25 Brazilian cases.
Albano LM, Zatz M, Kim CA, Bertola D, Sugayama SM, Marques-Dias MJ, Kok F, Ferraretto I, Rosemberg S, Cocozza S, Monticelli A. Albano LM, et al. Among authors: kok f. Rev Hosp Clin Fac Med Sao Paulo. 2001 Sep-Oct;56(5):143-8. doi: 10.1590/s0041-87812001000500003. Rev Hosp Clin Fac Med Sao Paulo. 2001. PMID: 11781594
Spastic paraplegia, optic atrophy, and neuropathy: new observations, locus refinement, and exclusion of candidate genes.
Macedo-Souza LI, Kok F, Santos S, Licinio L, Lezirovitz K, Cavaçana N, Bueno C, Amorim S, Pessoa A, Graciani Z, Ferreira A, Prazeres A, de Melo AN, Otto PA, Zatz M. Macedo-Souza LI, et al. Among authors: kok f. Ann Hum Genet. 2009 May;73(Pt 3):382-7. doi: 10.1111/j.1469-1809.2009.00507.x. Epub 2009 Mar 4. Ann Hum Genet. 2009. PMID: 19344448
621 results