login


Cadastre-se aqui
senha
 

Esqueceu sua senha?

Home
Controle de qualidade
Curriculum do diretor
Publicações científicas
Artigos
Genetika na mídia
Localização
Contato
Exames oferecidos
Solicitação de exames
Planos de Saúde
Aconselhamento
Teste de Paternidade
Banco de DNA
Pesquisa genética
Cadastre-se
Sugestão/reclamação
Cadastre seu curriculum
ROL ANS 2016
CBHPM
Galeria de Fotos
Projeto Genoma
CID Doenças genéticas
Associações de apoio
Login



  .: Publicações Científicas

Curriculum Lattes - Dr. Salmo Raskin: Clique Aqui

1. Faucz FR, Souza DA, Olandoski M, Raskin S.
CFTR allelic heterogeneity in Brazil: historical and geographical perspectives and implications for screening and counseling for cystic fibrosis in this country. / Journal of Human Geneticsver resumo
2. Renato P. Munhoz, Helio A. Teive, Alexandre N. Francisco, Salmo Raskin, Ekaterina Rogaeva
Unilateral pallidotomy in a patient with parkinsonism and G2019S LRRK2 mutation / Wiley InterScience: Movement Disorders / 2009 Apr 15;24(5):791-2ver resumo
3. Munhoz RP, Teive HA, Raskin S, Werneck LC
CTA/CTG expansions at the SCA 8 locus in multiple system atrophy / Clinical Neurology and Neurosurgery / 2009 Feb;111(2):208-10ver resumo
4. Zechi-Ceide RM, Ribeiro LA, Raskin S, Bertolacini CD, Guion-Almeida ML, Richieri-Costa A
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes / American Journal of Medical Geneticsver resumo
5. Guilherme G. Riccioppo Rodrigues, Ruth H. Walker, Alexis, Brice, Cécile Cazeneuve, Odile Russaouen, Helio A.G. Teive, Renato Puppi Munhoz, Nilson Becker, Salmo Raskin, Lineu Cesar Werneck, Wilson Marques Junior and Vitor Tumas
Huntington's Disease-Like 2 in Brazil - Report of 4 Patients / Mov Disord.23(15):2244-7.ver resumo arquivo
6. M. L. F. Santos & S. Raskin & D. S. Telles & A. Löhr Junior & P. B. N. Liberalesso & S. C. Vieira & M. L. Cordeiro
Treatment of a child diagnosed with Niemann-Pick disease type C with miglustat: A case report in Brazil / Journal of Inherited Metabolic Disease / 21 October 2008 ver resumo arquivo
7. Teive HA, Munhoz RP, Muzzio JA, Scola RH, Kay CK, Raskin S, Werneck LC, Bruhn H.
Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report. / Mov Disord. 2008 Apr 15;23(8):1191-1192ver resumo
8. Munhoz RP, Wakutani Y, Marras C, Teive HA, Raskin S, Werneck LC, Moreno D, Sato C, Lang AE, Rogaeva E.
The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: Phenotype in monozygotic twins. / Mov Disord. 2008 Jan 30;23(2):290-4. ver resumo
9. Salmo Raskin, Lilian Pereira Ferrari, Francisco Caldeira Reis, Fernando Abreu, Paulo Marostica, Tatiana Rozov, Joselina Cardieri, Norberto Ludwig, Lairton Valentin, Nelson Augusto Rosario-Filho, Eurico Camargo Neto, Eduardo Lewis, Roberto Giugliani, Edna Maria Albuquerque Diniz, Lodercio Culpi, John Atlas Phillip III, Ranajit Chakraborty
Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients / Journal of Cystic Fibrosis 7 (2008) 15–22ver resumo
10. Teive HA, Arruda WO, Raskin S, Ashizawa T, Werneck LC.
The history of spinocerebellar ataxia type 10 in Brazil: travels of a gene. / Arq Neuropsiquiatr. 2007 Dec;65(4A):965-8. ver resumo
11. Faucz FR, Gimenez J, Ramos MD, Pereira-Ferrari L, Estivill X, Raskin S, Casals T, Culpi L.
Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles. / Clin Genet. 2007 Sep;72(3):218-23ver resumo
12. Becker N, Munhoz RP, Raskin S, Werneck LC, Teive HA.
Non-choreic movement disorders as initial manifestations of Huntington's disease / Arq Neuropsiquiatr. 2007 Jun;65(2B):402-5.ver resumo
13. S. Raskin, M. L. Petzel-Erler, J.A. Phillips III, L. Pereira-Ferrari, C.M. Probst, F.R. Faucz, V. Sotomaior, F. M. Salzano and L. Culpi.
Cystic Fibrosis Gene Variability in Two Southern Brazilian Amerindian Populations: Analysis of the F508 Mutation and the KM19 and XV2C Haplotypes /  arquivo
14. Raskin S, Ashizawa T, Teive HA, Arruda WO, Fang P, Gao R, White MC, Werneck LC, Roa B.
Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10. / Arch Neurol. 2007 Apr;64(4):591-4. ver resumo
15. Stachon A, Assumpcao FB Jr, Raskin S.
Rett syndrome: clinical and molecular characterization of two Brazilian patients.Rett syndrome: clinical and molecular characterization of two Brazilian patients. / Arq Neuropsiquiatr. 2007 Mar;65(1):36-40. ver resumo
16. Raskin S, Petzl-Erler M L, Phillips J A, Pereira-Ferrari L, Probst C M, Faucz F R, Sotomaior V, Salzano Francisco M, Culpi L.
Cystic Fibrosis Gene Variability in Two Southern Brazilian Amerindian Populations: Analysis of the ÄF508 Mutation and the KM19 and XV2C Haplotypes / Human Biology - Volume 79, Number 1, February 2007, pp. 79-91 ver texto
17. Zenker M, Lehmann K, Schulz AL, Barth H, Hansmann D, Koenig R, Korinthenberg R, Kreiss-Nachtsheim M, Meinecke P, Morlot S, Mundlos S, Quante AS, Raskin S, Schnabel D, Wehner LE, Kratz CP, Horn D, Kutsche K
Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations. / J Med Genet. 2006 Oct 20;ver resumo ver texto
18. Carrara RC, Yamasaki R, Bragança W, Raskin S, Sartorato EL, Pina-Neto JM.
Etiologic investigations on male infertility before intracytoplasmatic sperm injection (ICSI). / Genet Couns. 2006;17(3):385-9. ver resumo
19. Munhoz RP, Kawarai T, Teive HA, Raskin S, Sato C, Liang Y, St George-Hyslop PH, Rogaeva E.
Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus). / Mov Disord. 2006 Feb;21(2):279-81.ver resumo
20. Gomide P ; MILLAN, D. ; BOARON, M. ; RASKIN, S.
Práticas parentais educativas e gravidez na adolescência / Revista Médica do Paraná, v. 63, p. 32-36, 2006
21. Munhoz RP, Teive HA, Raskin S, Troiano AR.
Atypical parkinsonism and SCA8. / Parkinsonism Relat Disord. 2005 Dec 17ver resumo ver texto
22. Polityko A, Starke H, Rumyantseva N, Claussen U, Liehr T, Raskin S.
Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding / Cytogenet Genome Res. 2005;111(2):171-4. ver resumo ver texto
23. Munhoz RP, Kawarai T, Teive HA, Raskin S, Sato C, Liang Y, St George-Hyslop PH, Rogaeva E.
Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus / Mov Disord. 2005 Nov 2;ver resumo ver texto
24. Raskin, Salmo; Crensiglova, Wagner; Malafaia, Osvaldo; Czeczko, Nicolau Gregori; Paciornik, Ester F.
O papel da genética no envelhecimento: implicações na qualidade de vida do idoso / Rev. med. Parana;63(2):5-9, jul.-dez. 2005.ver resumo
25. Mariane L. Bonato, Salmo Raskin, Rosa Maria Marini Mariotto, Fabio R. Faucz
O IMPACTO PSICOLÓGICO DO DIAGNÓSTICO POSITIVO DO TESTE DO PEZINHO NA RELAÇÃO MÃE–BEBÊ / v.27 n.60 Jul /Set. 2005ver resumo ver texto
26. Kurotaki N, Shen JJ, Touyama M, Kondoh T, Visser R, Ozaki T, Nishimoto J, Shiihara T, Uetake K, Makita Y, Harada N, Raskin S, Brown CW, Hoglund P, Okamoto N, Lupski JR.
Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency / Genet Med. 2005 Sep;7(7):479-83. ver resumo ver texto
27. Trentin AP, Scola RH, Teive HA, Raskin S, Germiniani FM, Werneck LC.
Kennedy's disease phenotype with positive genetic study for Kugelberg-Welander's disease: case report. / Arq Neuropsiquiatr. 2005 Jun;63(2A):330-1. ver resumo ver texto
28. Monalisa Castilho Mendes, Ilan Goldenstein, Salmo Raskin, Fábio Rueda Faucz
Confronto Entre Suspeitas Diagnósticas Para Alterações Cromossômicas e Confirmações Laboratoriais: Um Retrospecto de 1995 a 2003 / Revista Estudos de Biologia, v.26 , n.57, p.41-48, out./dez. 2004 arquivo
29. Teive HA, Pereira ER, Zavala JA, Lange MC, de Paola L, Raskin S, Werneck LC, Hamada T, McGrath JA.
Generalized dystonia and striatal calcifications with lipoid proteinosis. / Neurology. 2004 Dec 14;63(11):2168-9. PMID: 15596773ver resumo ver texto
30. Lange MC, Zetola VF, Teive HA, Scola RH, Trentin AP, Zavala JA, Pereira ER, Raskin S, Werneck LC, Sistermans EA.
Cerebrotendinous xanthomatosis: report of two Brazilian brothers. / Arq Neuropsiquiatr. 2004 Dec;62(4):1085-9.ver resumo ver texto
31. Isabelle Rego Barros, Salmo Raskin, Lilian Pereira-Ferrari
Dystrophic Epydermolisis Bullosa: Report of a brazilian case / Estud. Biol. v.26 n.57 out./dez. 2004  ver texto
32. Isabelle Rego Barros, Salmo Raskin, Lilian Pereira-Ferrari
Epidermólise bolhosa distrófica: relato de um caso brasileiro / Estud. Biol. v.26 n.57 out./dez. 2004 ver resumo
33. Teive HA, Troiano AR, Raskin S, Werneck LC.
Leber's hereditary optic neuropathy--case report and literature review. / Sao Paulo Med J. 2004 Nov 4;122(6):276-9ver resumo ver texto
34. Teive HA, Roa BB, Raskin S, Fang P, Arruda WO, Neto YC, Gao R, Werneck LC, Ashizawa T.
Clinical phenotype of Brazilian families with spinocerebellar ataxia 10. / Neurology. 2004 Oct 26;63(8):1509-12. PMID: 15505178ver resumo ver texto
35. Pedro A. Kowacs, Elcio J. Piovesan, Lineu C. Werneck, Hudson Fameli, Marcos C. Lange and Salmo Raskin
Report of cluster headache in a pair of monozygous twins / The Journal of Headache and Pain, Volume 5, Number 2 / August, 2004ver resumo
36. Coutinho G, Mitui M, Campbell C, Costa Carvalho BT, Nahas S, Sun X, Huo Y, Lai CH, Thorstenson Y, Tanouye R, Raskin S, Kim CA, Llerena J Jr, Gatti RA.
Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: seven new mutations. / Am J Med Genet. 2004 Apr 1;126A(1):33-40. PMID: 15039971 [PubMed - indexed for MEDLINE]ver resumo ver texto
37. Kamimura J, Endo Y, Kurotaki N, Kinoshita A, Miyake N, Shimokawa O, Harada N, Visser R, Ohashi H, Miyakawa K, Gerritsen J, Innes AM, Lagace L, Frydman M, Okamoto N, Puttinger R, Raskin S, Resic B, Culic V, Yoshiura K, Ohta T, Kishino T, Ishikawa M, Niikawa N, Matsumoto N.
Identification of eight novel NSD1 mutations in Sotos syndrome. / J Med Genet. 2003 Nov;40(11):e126. No abstract available. PMID: 14627693 [PubMed - indexed for MEDLINE]ver resumo ver texto
38. Lohmann E, Periquet M, Bonifati V, Wood NW, De Michele G, Bonnet AM, Fraix V, Broussolle E, Horstink MW, Vidailhet M, Verpillat P, Gasser T, Nicholl D, Teive H, Raskin S, Rascol O, Destee A, Ruberg M, Gasparini F, Meco G, Agid Y, Durr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.
How much phenotypic variation can be attributed to parkin genotype? / Ann Neurol. 2003 Aug;54(2):176-85. PMID: 12891670 [PubMed - indexed for MEDLINE]ver resumo ver texto
39. Raskin S, Pereira L, Reis F, Rosario NA, Ludwig N, Valentim L, Phillips JA 3rd, Allito B, Heim RA, Sugarman EA, Probst C, Faucz F, Culpi L.
High allelic heterogeneity between Afro-Brazilians and Euro-Brazilians impacts cystic fibrosis genetic testing. / Genet Test. 2003 Fall;7(3):213-8. PMID: 14641997 [PubMed - indexed for MEDLINE]ver resumo ver texto
40. Silva Filho LV, Bussamra MH, Nakaie CM, Adde FV, Rodrigues JC, Raskin S, Rozov T.
Cystic fibrosis with normal sweat chloride concentration: case report. Rev Hosp Clin Fac Med Sao Paulo. / 2003 Sep-Oct;58(5):260-2ver resumo ver texto
41. Claes L, Ceulemans B, Audenaert D, Smets K, Lofgren A, Del-Favero J, Ala-Mello S, Basel-Vanagaite L, Plecko B, Raskin S, Thiry P, Wolf NI, Van Broeckhoven C, De Jonghe P.
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy. / Hum Mutat. 2003 Jun;21(6):615-21. PMID: 12754708 [PubMed - indexed for MEDLINE]ver resumo ver texto
42. Periquet M, Latouche M, Lohmann E, Rawal N, De Michele G, Ricard S, Teive H, Fraix V, Vidailhet M, Nicholl D, Barone P, Wood NW, Raskin S, Deleuze JF, Agid Y, Durr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.
Parkin mutations are frequent in patients with isolated early-onset parkinsonism. / Brain. 2003 Jun;126(Pt 6):1271-8. PMID: 12764050 [PubMed - indexed for MEDLINE]ver resumo ver texto
43. Goloni-Bertollo EM, Rossit AR, Junior JB, Fett-Conte AC, Raskin S.
CFTR molecular analysis reveals infrequent allele frequencies in nine cystic fibrosis patients from Sao Paulo State, Brazil. / Hum Biol. 2003 Jun;75(3):393-8. Review. PMID: 14527202 [PubMed - indexed for MEDLINE]ver resumo ver texto
44. Rawal N, Periquet M, Lohmann E, Lucking CB, Teive HA, Ambrosio G, Raskin S, Lincoln S, Hattori N, Guimaraes J, Horstink MW, Dos Santos Bele W, Brousolle E, Destee A, Mizuno Y, Farrer M, Deleuze JF, De Michele G, Agid Y, Durr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.
New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism. / Neurology. 2003 Apr 22;60(8):1378-81. PMID: 12707451 [PubMed - indexed for MEDLINE]ver resumo ver texto
45. Lee HH, Chang SF, Lee YJ, Raskin S, Lin SJ, Chao MC, Lo FS, Lin CY.
Deletion of the C4-CYP21 repeat module leading to the formation of a chimeric CYP21P/CYP21 gene in a 9.3-kb fragment as a cause of steroid 21-hydroxylase deficiency. / Clin Chem. 2003 Feb;49(2):319-22. No abstract available. PMID: 12560361 [PubMed - indexed for MEDLINE]ver resumo ver texto
46. Sun G, McGarvey ST, Bayoumi R, Mulligan CJ, Barrantes R, Raskin S, Zhong Y, Akey J, Chakraborty R, Deka R.
Global genetic variation at nine short tandem repeat loci and implications on forensic genetics. / Eur J Hum Genet. 2003 Jan;11(1):39-49. PMID: 12529704 [PubMed - indexed for MEDLINE]ver resumo ver texto
47. Rawal N, Periquet M, Durr A, de Michele G, Bonifati V, Teive HA, Raskin S, Guimaraes J, Agid Y, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.
Exclusion of the Nurr1 gene in autosomal recessive Parkinson's disease. / J Neurol. 2002 Aug;249(8):1127-9. No abstract available. PMID: 12420720 [PubMed - indexed for MEDLINE]ver resumo ver texto
48. Camacho S ; RASKIN, S.
APRESENTAÇÃO DE CASO CLÍNICO - SINDROME DE SECKEL / Endocrinologia & diabetes clínica e experimental, v. 4, p. 180-182
49. RASKIN, S.
O mapeamento genético de pit-1 em humanos: o gene dos genes. / Endocrinologia & diabetes clínica e experimental, v. 2, p. 47-48, 2002.
50. Teive HA, Raskin S, Iwamoto FM, Germiniani FM, Baran MH, Werneck LC, Allan N, Quagliato E, Leroy E, Ide SE, Polymeropoulos MH.
The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease. / Arq Neuropsiquiatr. 2001 Sep;59(3-B):722-4ver resumo ver texto
51. Kwok JB, Raskin S, Morgan G, Antoniuk SA, Bruk I, Schofield PR.
Mutations in the glycine receptor alpha1 subunit (GLRA1) gene in hereditary hyperekplexia pedigrees: evidence for non-penetrance of mutation Y279C. / J Med Genet. 2001 Jun;38(6):E17. No abstract available.PMID: 11389164 [PubMed - indexed for MEDLINE]ver resumo ver texto
52. Scola RH, Werneck LC, Iwamoto FM, Ribas LC, Raskin S, Correa Neto Y.
Congenital contractural arachnodactyly with neurogenic muscular atrophy: case report. / Arq Neuropsiquiatr. 2001 Jun;59(2-A):259-62.ver resumo ver texto
53. Raskin S, Allan N, Teive HA, Cardoso F, Haddad MS, Levi G, Boy R, Lerena Junior J, Sotomaior VS, Janzen-Duck M, Jardim LB, Fellander FR, Andrade LA.
Huntington disease: DNA analysis in Brazilian population. / Arq Neuropsiquiatr. 2000 Dec;58(4):977-85.PMID: 11105061 [PubMed - indexed for MEDLINE]ver resumo ver texto
54. O'Neill P, Trombley L, Gundel M, Hunter T, Nicklas JA, Ferreira ML, Bugallo MJ, Farias AC, Lohr A, Diamantopoulos M, Raskin S.
Identification of a new Lesch-Nyhan syndrome mutation (HPRTBrasil) and analysis of potentially heterozygous females. / Arq Neuropsiquiatr. 1999 Dec;57(4):907-11.PMID: 10683677 [PubMed - indexed for MEDLINE]ver resumo ver texto
55. Levy G, Nobre ME, Cimini VT, Raskin S, Engelhardt E.
Juvenile Huntington's disease confirmed by genetic examination in twins. / Arq Neuropsiquiatr. 1999 Sep;57(3B):867-9.PMID: 10751926 [PubMed - indexed for MEDLINE]ver resumo ver texto
56. Noronha L, Sampaio G, Netto MR, Reis-Filho JS, Faoro LN, Raskin S, Bleggi-Torres LF.
[Neurocutaneous melanosis] J Pediatr (Rio J). / 1999 Jul-Aug;75(4):277-80. Portuguese. PMID: 14685530ver resumo ver texto
57. PEREIRA, Lilian, RASKIN, Salmo, FREUND, Aline A.
Cystic fibrosis mutations R1162X and 2183AA->G in two southern Brazilian States / Genet. Mol. Boil. v.22 n.3 São Paulo set. 1999ver resumo ver texto
58. Almeida DB, Arruda WO, Ramina R, Pedrozo AA, Raskin S.
Migraine with aphasia. Report of a family / Arq Neuropsiquiatr. 1999 Mar;57(1):111-3. Portuguese.PMID: 10347736 [PubMed - indexed for MEDLINE]ver resumo ver texto
59. Raskin S, Phillips JA, Kaplan G, McClure M, Vnencak-Jones C, Rozov T, Cardieri JM, Marostica P, Abreu F, Giugliani R, Reis F, Rosario NA, Ludwig N, Pereira L, Faucz F, Gabardo J, Culpi L.
Geographic heterogeneity of 4 common worldwide cystic fibrosis non-DF508 mutations in Brazil. / Hum Biol. 1999 Feb;71(1):111-21.PMID: 9972102 [PubMed - indexed for MEDLINE]ver resumo ver texto
60. O'nneil P ; RASKIN, S. ; TROMBLEY, L. ; GUNDEL, M. ; HUNTER, Y. ; NICKLAS, J. A. ; FERREIRA, M. L. ; BUGALO, M. ; FARIAS, A. C. ; LOHR, A. ; DIAMANTOPOULOS, M. . Identification of a new Lesh-Nyhan syndrome mutation (HPRTBrasil) and analysis of potencially heterozygous female. Arquivos de Neuro-Psiquiatria, v. 57, n. 4, p. 907-911, 1999.
Identification of a new Lesh-Nyhan syndrome mutation (HPRTBrasil) and analysis of potencially heterozygous female. / Arquivos de Neuro-Psiquiatria, v. 57, n. 4, p. 907-911, 1999ver resumo
61. Zetola VH, Scola RH, Raskin S, Prevendello DM, Correa Neto Y, Werneck LC.
Rigid spine syndrome. Case report. / Arq Neuropsiquiatr. 1998 Dec;56(4):812-8.PMID: 10029887 [PubMed - indexed for MEDLINE]ver resumo ver texto
62. Kaimen-Maciel DR, Medeiros M, Climaco V, Kelian GR, da Silva LS, de Souza MM, Raskin S.
X-linked recessive bulbospinal muscular atrophy (Kennedy's disease). A family study. / Arq Neuropsiquiatr. 1998 Sep;56(3B):639-45. Portuguese.PMID: 9850762 [PubMed - indexed for MEDLINE]ver resumo ver texto
63. Marostica PJ, Raskin S, Abreu-e-Silva FA.
Analysis of the delta F508 mutation in a Brazilian cystic fibrosis population: comparison of pulmonary status of homozygotes with other patients. / Braz J Med Biol Res. 1998 Apr;31(4):529-32.PMID: 9698805 [PubMed - indexed for MEDLINE]ver resumo ver texto
64. Rodrigues Martineli AM, Braga M, De Lacerda L, Raskin S, Graf H.
Description of a Brazilian patient bearing the R271W Pit-1 gene mutation. / Thyroid. 1998 Apr;8(4):299-304.PMID: 9588494 [PubMed - indexed for MEDLINE]ver resumo ver texto
65. Burger M, Raskin S, Brockelt SR, Amthor B, Geiss HK, Haas WH.
DNA fingerprinting of Mycobacterium tuberculosis complex culture isolates collected in Brazil and spotted onto filter paper. / J Clin Microbiol. 1998 Feb;36(2):573-6.PMID: 9466780 [PubMed - indexed for MEDLINE]ver resumo ver texto
66. Raskin S, Phillips JA 3rd, Krishnamani MR, Vnencak-Jones C, Parker RA, Rozov T, Cardieri JM, Marostica P, Abreu F, Giugliani R, Reis F, Rosario NA, Ludwig N, Culpi L.
Cystic fibrosis in the Brazilian population: DF508 mutation and KM-19/XV-2C haplotype distribution. / Hum Biol. 1997 Aug;69(4):499-508.PMID: 9198309 [PubMed - indexed for MEDLINE]ver resumo ver texto
67. Raskin S, Leal M. F
Validade da Técnica de PCR-STR na Determinação de Paternidade em DNA / Laes & Haes, v. 34, p. 100, 1997 arquivo
68. Raskin S, Philips JA 3rd, Krishnamani MR, Vnencak-Jones C, Parker RA, Dawson E, Rozov T, Cardieri JM, Marostica P, Abreu F, Giugliani R, Reis F, Rosario NA, Ludwig N, Culpi L.
Regional distribution of cystic fibrosis-linked DNA haplotypes in Brazil: multicenter study. / Hum Biol. 1997 Feb;69(1):75-88.PMID: 9037896 [PubMed - indexed for MEDLINE]ver resumo ver texto
69. RASKIN, S.
Avaliação do Risco Fetal por Uma Gota de Sangue em Papel Filtro / Newslab, v. 18, p. 130-131, 1997 arquivo
70. Raskin S, Cogan JD, Summar ML, Moreno A, Krishnamani MR, Phillips JA 3rd.
Genetic mapping of the human pituitary-specific transcriptional factor gene and its analysis in familial panhypopituitary dwarfism. / Hum Genet. 1996 Dec;98(6):703-5.PMID: 8931705 [PubMed - indexed for MEDLINE]ver resumo ver texto
71. Raskin S, Cogan JD, Summar ML, Moreno A, Krishnamani MR, Phillips JA 3rd.
Genetic mapping of the human pituitary-specific transcriptional factor gene and its analysis in familial panhypopituitary dwarfism. / Hum Genet. 1996 Dec;98(6):703-5ver resumo
72. Rogan PK, Seip JR, Driscoll DJ, Papenhausen PR, Johnson VP, Raskin S, Woodward AL, Butler MG.
Distinct 15q genotypes in Russell-Silver and ring 15 syndromes. / Am J Med Genet. 1996 Mar 1;62(1):10-5.PMID: 8779316 [PubMed - indexed for MEDLINE]ver resumo ver texto
73. RASKIN, S.
Teste de DNA para a Doença de Alzheimer / O Dendrito, v. Ano 3, n. 3, p. 321-3223, 1996
74. Deka R, Miki T, Yin SJ, McGarvey ST, Shriver MD, Bunker CH, Raskin S, Hundrieser J, Ferrell RE, Chakraborty R.
Normal CAG repeat variation at the DRPLA locus in world populations. / Am J Hum Genet. 1995 Aug;57(2):508-11. No abstract available.PMID: 7668279 [PubMed - indexed for MEDLINE]ver resumo ver texto
75. Maróstica, Paulo José Cauduro; Santos, Jacqueline Almeida; Souza, Wilma Adriane Sulzbach de; Raskin, Salmo; Silva, Fernando Antonio de Abreu e
Estimativa da incidência de fibrose cística em Porto Alegre: análise a partir da frequência da mutaçäo delta F508 em recém-nascidos normais / Rev. AMRIGS;39(3):205-7, jul.-set. 1995ver resumo
76. RASKIN, S.
Ética e Genética. / Educar em revista, v. 11, p. 27-32, 1995
77. HAMOSH, A. ; ROSENSTEIN, B. ; NASH, E. ; CURRISTIN, S. ; CUTTING, G. ; MACEK JR, M. ; MCINTOSH, I. ; RASKIN, S
Correlation Between Genotype and Phenotype in Patients With Cystic Fibrosis. / N Engl J Med. 1993 Oct 28;329(18):1308-13.ver resumo
78. Raskin S, Phillips JA 3rd, Krishnamani MR, Vnencak-Jones C, Parker RA, Rozov T, Cardieri JM, Marostica P, Abreu F, Giugliani R, et al.
DNA analysis of cystic fibrosis in Brazil by direct PCR amplification from Guthrie cards. / Am J Med Genet. 1993 Jul 1;46(6):665-9.PMID: 8362909 [PubMed - indexed for MEDLINE]ver resumo ver texto
79. Chakraborty R, Srinivasan MR, Raskin S.
Estimation of the incidence of a rare genetic disease through a two-tier mutation survey. / Am J Hum Genet. 1993 Jun;52(6):1129-38.PMID: 8503445 [PubMed - indexed for MEDLINE]ver resumo ver texto
80. TAYLOR, B.A. ; RASKIN, S.
Mapping of a Pit-1 PCR-RFLV in Recombinant Inbred Strains. / Mouse Genome, v. 91, n. 1, p. 134-136, 1993.
81. Raskin S, Phillips JA 3rd, Kaplan G, McClure M, Vnencak-Jones C.
Cystic fibrosis genotyping by direct PCR analysis of Guthrie blood spots. / PCR Methods Appl. 1992 Nov;2(2):154-6.PMID: 1362128 [PubMed - indexed for MEDLINE]ver resumo ver texto
82. Molina Cabanero JC, Perez Jurado LA, Raskin S, Vicario JL, Balas Perez A, Garcia Novo MD.
Simple method for cystic fibrosis carrier screening. / Lancet. 1992 Oct 17;340(8825):983-4. No abstract available.PMID: 1357395 [PubMed - indexed for MEDLINE]ver resumo ver texto
83. Raskin S, Phillips JA 3rd, Vnencak-Jones C, Dawson E, Kaplan G, McClure M.
Utility of internal markers to improve the accuracy of cystic fibrosis genotype analysis. / Biotechniques. 1992 Sep;13(3):372-4.PMID: 1382468 [PubMed - indexed for MEDLINE]ver resumo ver texto
84. OSBORNE, L. ; Santis G ; M Schwarz ; M Klinger ; RASKIN, S.
. Incidence and Expression of the N1303K Mutation of the Cystic Fibrosis (CFTR) Gene / Hum Genet. 1992 Aug;89(6):653-8.ver resumo
85. RASKIN, S. ; PHILLIPS, J. A.
Genetic Diagnosis of Cystic Fbrosis in the Perinatal Period / Tennessee Perinatal Association, v. 2, n. 1, p. 6-6, 1992.
86. Luiz, Albano Manuel de Almeida Chaves; Vieira, Maria Cristina Gomes; Raskin, Salmo
A síndrome de Dressler: um diagnóstico esquecido? / Revista Médica do Paraná, v. 46, n. 1, p. 7-10, 1988ver resumo