Publicaciones
Rodriguez S, Córdoba M, Gonzalez-Morón D, Medina N, Vega P, Vazquez Dusefante C, Arakaki T, Garretto N, Kauffman MA.
Neurogenetics in Argentina: Diagnostic Yield in a Personalized Research Based Clinic (2015). Genetics Research (in press)
Nemirovsky SI, Córdoba M, Zaiat JJ, Completa SP, Vega PA, González-Morón D, Medina NM, Fabbro M, Romero S, Brun B, Revale S, Ogara MF, Pecci A, Marti M, Vazquez M, Turjanski A, Kauffman MA. Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder (2015). PLoS One Feb 3;10(2):e0116358. [Download] [Pubmed]
Córdoba M, Rodriguez S, González Morón D, Medina N, Kauffman MA. Expanding the spectrum of Grik2 mutations: intellectual disability, behavioural disorder, epilepsy and dystonia (2015). Clin Genet. 87:293-5. [Download] [Pubmed]
Wolf NI, Vanderver A, van Spaendonk RM, Schiffmann R, Brais B, Bugiani M, Sistermans E, Catsman-Berrevoets C, Kros JM, Pinto PS, Pohl D, Tirupathi S, Strømme P, de Grauw T, Fribourg S, Demos M, Pizzino A, Naidu S, Guerrero K, van der Knaap MS, Bernard G; 4H Research Group (miembro de Research Group). Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations (2014). Neurology 83:1898-905. [Download] [Pubmed]
Cordoba M, Rodriguez-Quiroga S, Gatto EM, Alurralde A, Kauffman MA. Ataxia plus myoclonus in a 23-year-old patient due to STUB1 mutations (2014). Neurology 83:287-8. [Download] [Pubmed]
Córdoba M, González Morón D, Rodríguez-Quiroga S, Kauffman MA (2014). Neurología genómica personalizada: el futuro es ahora. Neurol Arg 6:127-36. [Download]
Consalvo D, Kauffman MA, Oddo S, Pereira de Silva N, Kochen S (2014). Imágenes por resonancia magnética anormales como predictoras de mal pronóstico en epilepsia focal. Neurol Arg 6:61-7. [Download]
Rodríguez-Quiroga SA, González-Morón D, Arakaki T, Garreto N, Kauffman MA. [The broad phenotypic spectrum of SCA-3: hereditary spastic paraplegia] (2013). Medicina (B Aires) 73:552-4. [Download] [Pubmed]
Gonzalez-Moron D, Bueri J, Kauffman MA. Progressive external ophthalmoplegia (PEO) due to a mutation in the C10orf2 (PEO1) gene mimicking a myasthenic crisis (2013). BMJ Case Rep. Sep 7;2013. pii: bcr2013010181. [Download] [Pubmed]
Rodríguez-Quiroga SA, Gonzalez-Morón D, Garretto N, Kauffman MA. Huntington's disease masquerading as spinocerebellar ataxia (2013). BMJ Case Rep. Jul 12;2013. pii: bcr2012008380. [Download] [Pubmed]
Hirose S, Scheffer IE, Marini C, De Jonghe P, Andermann E, Goldman AM, Kauffman M, Tan NC, Lowenstein DH, Sisodiya SM, Ottman R, Berkovic SF; Genetics Commission of the International League Against Epilepsy (2013). SCN1A testing for epilepsy: application in clinical practice. Epilepsia 54:946-52. [Download] [Pubmed]
Kauffman MA (2012). Tres Preguntas y una Respuesta: Algoritmo Diagnóstico Molecular en Enfermedades Mitocondriales. Neurol Arg 5:19-26. [Download]
Consalvo D, Kauffman MA, Oddo S, Rey R, Kochen S (2012). Alteraciones extrahipocámpicas en epilepsia temporal. Neurol Arg 4:53-58 [Download]
Papayannis C, Consalvo D, Kauffman MA, Seifer G, Oddo S, D´Alessio L, Saidon P, Kochen S (2012). Malformations of cortical development and epilepsy in adult patients. Seizure 21(5):377-84. [Download] [Pubmed]
Cordoba M, Consalvo D, Gonzalez Moron D, Kochen S, Kauffman MA (2012). SLC6A4 gene variants and temporal lobe epilepsy susceptibility: a meta-analysis. Mol Biol Rep. 39(12):10615-9 [Download] [Pubmed]
Kauffman MA (2012). Algunas reflexiones sobre genomas e información genética en Babel y Buenos Aires. Neurol Arg 4(1):1-2 [Download]
Kauffman MA, Gonzalez-Morón D, Consalvo D, Westergaard G, Vazquez M, Mancini E, Taratuto AL, Rey RC, Kochen S (2012). Diagnosis of mitochondrial disorders applying massive pyrosequencing. Mol Biol Rep. 39(6):6655-60 [Download] [Pubmed]
Princich JP, Consalvo D, Kauffman MA, Seifer G, Blenkmann A, Kochen S (2012). Contribution of diffusion tensor magnetic resonance imaging to the diagnosis of focal cortical dysplasias. Rev Neurol 54(8):453-60. [Download] [Pubmed]
Kauffman MA, Gonzalez-Morón D, Consalvo D, Kochen S (2012). Cerebrotendinous Xanthomatosis Revealed in Drug-Resistant Epilepsy Diagnostic Workup. Am J Med Sci. 343(4):332-333 [Download] [Pubmed]
Abaroa L, Garretto NS, Arakaki T, Kauffman M, Moron DG, Figueredo AM, Szlago M, Metman LV (2011). Myoclonus and angiokeratomas in adult galactosialidosis. Mov Disord. 26(4):756-7 [Download] [Pubmed]
Kauffman MA, Sterin-Prync A, Papouchado M, Gonzalez E, Vidal AJ, Grossberg SE, Chuppa S, Odoriz B, Vrech C, Diez RA, Ferro HH (2011). Immunogenicity of an interferon-beta1a product. Int J Immunopathol Pharmacol, 24(2):499-504 [Download] [Pubmed]
Kauffman MA, Gonzalez-Morón D, Garcea O, Villa AM (2011). TNFSFR1A R92Q mutation, autoinflammatory symptoms and multiple sclerosis in a cohort from Argentina. Mol Biol Rep. 39(1):117-21 [Download] [Pubmed]
Kauffman MA, Consalvo D, Gonzalez-Morón D, Pujol V, Kochen S (2010). ApoEε4 genotype and the age at onset of temporal lobe epilepsy: A case-control study and meta-analysis. Epilepsy Res, 90; 234-239 [Download] [Pubmed]
Gonzalez Morón D,Kauffman M, Garcea O, Villa AM (2010). Nuevos factores genéticos en la esclerosis múltiple: mutación R92Q en el gen TNFRSF1A y el síndrome autoinflamatorio TRAPS. Neurología Argentina 2; 29-34 [Download]
Kauffman MA, Consalvo D, Gonzalez-Morón D, Pujol V, Solís P, Oddo S, Lomlomdjian C, Kochen S (2009). El alelo e4 de la apolipoproteína e modificaría el “período silente” del desarrollo de la epilepsia mesial temporal con esclerosis del hipocampo. Neurología Argentina 1; 148-154 [Download]
Kauffman MA, Yankilevich P, Barrero P, Bello R, Marangunich L, Vidal A, Criscuolo M, Diez RA, SterinPrync A (2009). Whole genome analysis of the action of interferon-beta. Int J Clin PharmacolTher, 47; 328-57 [Download] [Pubmed]
Kauffman MA, Villa AM (2009). Comment to Tumour necrosis factor alpha gene -376 polymorphism in Hungarian patients with primary progressive multiple sclerosis. J Neuroimmunol, 212; 151 [Download] [Pubmed]
Kauffman MA, Consalvo D, Gonzalez-Morón D, Aguirre F, D'Alessio L, Kochen S (2009). Serotonin transporter gene variation and refractory mesial temporal epilepsy with hippocampal sclerosis. Epilepsy Res, 85; 231-234 [Download] [Pubmed]
Kauffman MA, Pereira-de-Silva N, Consalvo D, Kochen S (2009). ApoE epsilon4 is not associated with posictal confusion in patients with mesial temporal lobe epilepsy with hippocampal sclerosis. Epilepsy Res, 85; 311-313 [Download] [Pubmed]
Lahoz M, Kauffman M, Carfagnini J, Vidal A, Papouchado M, Sterin-Prync A, Diez R, Nagle C (2009). Pharmacokinetics and pharmacodynamics of interferon beta 1a in Cebus apella. J Med Primatol, 38; 187-191. [Download] [Pubmed]
D'Alessio L, Giagante B, Papayannis C, Oddo S, Silva W, Solís P, Donnoli V, Kauffman M, Consalvo D, Zieher LM, Kochen S (2009). Psychotic disorders in Argentine patients with refractory temporal lobe epilepsy: a case-control study. Epilepsy Behav, 14; 604-609 [Download] [Pubmed]
Melcon C, Consalvo D, Centurión E, Papayannis C, Kauffman M, Kochen S (2009). Heterotopía en banda o doble corteza. Reporte de caso. Neurología Argentina, 1; 47-49 [Download]
Arberas C, Aguirre F, Berardo A, GonzalezMoron D, Kauffman M, Maiola R, Melamud L, Pirra L, Seifer G (2008). Guías de Neurogenética de la Sociedad Neurológica Argentina. Rev Neurol Arg, 33; 86-94. [Download]
Kauffman M, Consalvo D, Gonzalez Morón D, Aguirre F, D´Alessio L, Kochen S (2008). Genotipificación del gen del recaptador de serotonina y respuesta al tratamiento en la epilepsia mesial temporal con esclerosis del hipocampo ¿pronóstico molecular?.Rev Neurol Arg, 33; 22-27. [Download]
Papayannis C, Consalvo D, Seifer G, Kauffman M, Silva W, Kochen S (2008). Clinical spectrum and difficulties in management of hypothalamic hamartoma in a developing country. Acta Neurol Scand,118: 313-19 [Download] [Pubmed]
Di Girolamo G, Kauffman M, Gonzalez E, Papouchado M, Ramírez A, Keller G, Carbonetto C, Dabsys S, Vidal A, Sterin-Prync A, Diez R (2008). Bioequivalence of Two Subcutaneous Pharmaceutical Products of Interferon Beta 1a. Drug Research, 58: 193-198 [Download] [Pubmed]
Kauffman M, Levy E, Consalvo D, Mordoh J, Kochen S (2008). GABABR1 (G1465A) gene variation and temporal lobe epilepsy controversy: new evidence. Seizure, 17; 567-71. [Download] [Pubmed]
Kauffman M, Consalvo D, Gonzalez Morón D, Kochen S (2008). Transcriptionally less active prodynorphin promoter alleles are associated with temporal lobe epilepsy: a case-control study and meta-analysis. Dis Markers, 24; 135-40. [Download] [Pubmed]
Kauffman M, Gonzalez Morón D, Consalvo D, Bello R, Kochen S (2008). Association study between interleukin 1β gene and epileptic disorders: a HuGe review and meta-analysis. Genetics in Medicine 10, 83-88. [Download] [Pubmed]
Prync AE, Yankilevich P, Barrero PR, Bello R, Marangunich L, Vidal A, Kauffman M, Diez RA (2008). Two recombinant human interferon-beta 1a pharmaceutical preparations produce a similar transcriptional response determined using whole genome microarrays analysis. Int J ClinPharmacolTher 46, 64-71 [Download] [Pubmed]
Kauffman M, Moron DG, Bruno V (2007). How accurate are bedside hearing test? Neurology 69 (13), 1382 [Download] [Pubmed]
Kauffman M, Gonzalez Morón D, Garcea O, Sica R, Villa AM (2007) Is tumour necrosis factor -376A promoter polymorphism associated with susceptibility to multiple sclerosis? Medicina (B Aires) 67 (5), 436-8. [Download] [Pubmed]
Kauffman M, Consalvo D, Kochen S. (2007) Genética de la Epilepsia del Lóbulo Temporal. Psicofarmacología, 7, 16-21. [Download]
Kauffman M, Consalvo D, GonzalezMoron D, Kochen S (2007) Asociación entre Alelos Transcripcionalmente Deficientes del gen de la Prodinorfina y el Desarrollo de Epilepsia del Lóbulo Temporal, Revista Neurológica Argentina, 32 (1), 40-46 [Download]
Kauffman M, Yankilevich P, Barrero P, SterynPrync A, Diez RA (2007) Caracterización de la expresión génica inducida por interferón beta en leucocitos de pacientes con Esclerosis Múltiple utilizando microarrays de genoma completo. Un Analisis Preliminar., Revista Neurológica Argentina, 32(2),105-117 [Download]
Kauffman M, Consalvo D, Levy E, Papayannis C, Mordoh J, Kochen S (2006) El Polimorfismo G1465A del Gen GABBR1 es un Marcador de Riesgo para el desarrollo de Epilepsia Mesial Temporal con Esclerosis del Hipocampo., Revista Neurológica Argentina, 31(1)25-31 [Download]
Neurogenetics in Argentina: Diagnostic Yield in a Personalized Research Based Clinic (2015). Genetics Research (in press)
Nemirovsky SI, Córdoba M, Zaiat JJ, Completa SP, Vega PA, González-Morón D, Medina NM, Fabbro M, Romero S, Brun B, Revale S, Ogara MF, Pecci A, Marti M, Vazquez M, Turjanski A, Kauffman MA. Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder (2015). PLoS One Feb 3;10(2):e0116358. [Download] [Pubmed]
Córdoba M, Rodriguez S, González Morón D, Medina N, Kauffman MA. Expanding the spectrum of Grik2 mutations: intellectual disability, behavioural disorder, epilepsy and dystonia (2015). Clin Genet. 87:293-5. [Download] [Pubmed]
Wolf NI, Vanderver A, van Spaendonk RM, Schiffmann R, Brais B, Bugiani M, Sistermans E, Catsman-Berrevoets C, Kros JM, Pinto PS, Pohl D, Tirupathi S, Strømme P, de Grauw T, Fribourg S, Demos M, Pizzino A, Naidu S, Guerrero K, van der Knaap MS, Bernard G; 4H Research Group (miembro de Research Group). Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations (2014). Neurology 83:1898-905. [Download] [Pubmed]
Cordoba M, Rodriguez-Quiroga S, Gatto EM, Alurralde A, Kauffman MA. Ataxia plus myoclonus in a 23-year-old patient due to STUB1 mutations (2014). Neurology 83:287-8. [Download] [Pubmed]
Córdoba M, González Morón D, Rodríguez-Quiroga S, Kauffman MA (2014). Neurología genómica personalizada: el futuro es ahora. Neurol Arg 6:127-36. [Download]
Consalvo D, Kauffman MA, Oddo S, Pereira de Silva N, Kochen S (2014). Imágenes por resonancia magnética anormales como predictoras de mal pronóstico en epilepsia focal. Neurol Arg 6:61-7. [Download]
Rodríguez-Quiroga SA, González-Morón D, Arakaki T, Garreto N, Kauffman MA. [The broad phenotypic spectrum of SCA-3: hereditary spastic paraplegia] (2013). Medicina (B Aires) 73:552-4. [Download] [Pubmed]
Gonzalez-Moron D, Bueri J, Kauffman MA. Progressive external ophthalmoplegia (PEO) due to a mutation in the C10orf2 (PEO1) gene mimicking a myasthenic crisis (2013). BMJ Case Rep. Sep 7;2013. pii: bcr2013010181. [Download] [Pubmed]
Rodríguez-Quiroga SA, Gonzalez-Morón D, Garretto N, Kauffman MA. Huntington's disease masquerading as spinocerebellar ataxia (2013). BMJ Case Rep. Jul 12;2013. pii: bcr2012008380. [Download] [Pubmed]
Hirose S, Scheffer IE, Marini C, De Jonghe P, Andermann E, Goldman AM, Kauffman M, Tan NC, Lowenstein DH, Sisodiya SM, Ottman R, Berkovic SF; Genetics Commission of the International League Against Epilepsy (2013). SCN1A testing for epilepsy: application in clinical practice. Epilepsia 54:946-52. [Download] [Pubmed]
Kauffman MA (2012). Tres Preguntas y una Respuesta: Algoritmo Diagnóstico Molecular en Enfermedades Mitocondriales. Neurol Arg 5:19-26. [Download]
Consalvo D, Kauffman MA, Oddo S, Rey R, Kochen S (2012). Alteraciones extrahipocámpicas en epilepsia temporal. Neurol Arg 4:53-58 [Download]
Papayannis C, Consalvo D, Kauffman MA, Seifer G, Oddo S, D´Alessio L, Saidon P, Kochen S (2012). Malformations of cortical development and epilepsy in adult patients. Seizure 21(5):377-84. [Download] [Pubmed]
Cordoba M, Consalvo D, Gonzalez Moron D, Kochen S, Kauffman MA (2012). SLC6A4 gene variants and temporal lobe epilepsy susceptibility: a meta-analysis. Mol Biol Rep. 39(12):10615-9 [Download] [Pubmed]
Kauffman MA (2012). Algunas reflexiones sobre genomas e información genética en Babel y Buenos Aires. Neurol Arg 4(1):1-2 [Download]
Kauffman MA, Gonzalez-Morón D, Consalvo D, Westergaard G, Vazquez M, Mancini E, Taratuto AL, Rey RC, Kochen S (2012). Diagnosis of mitochondrial disorders applying massive pyrosequencing. Mol Biol Rep. 39(6):6655-60 [Download] [Pubmed]
Princich JP, Consalvo D, Kauffman MA, Seifer G, Blenkmann A, Kochen S (2012). Contribution of diffusion tensor magnetic resonance imaging to the diagnosis of focal cortical dysplasias. Rev Neurol 54(8):453-60. [Download] [Pubmed]
Kauffman MA, Gonzalez-Morón D, Consalvo D, Kochen S (2012). Cerebrotendinous Xanthomatosis Revealed in Drug-Resistant Epilepsy Diagnostic Workup. Am J Med Sci. 343(4):332-333 [Download] [Pubmed]
Abaroa L, Garretto NS, Arakaki T, Kauffman M, Moron DG, Figueredo AM, Szlago M, Metman LV (2011). Myoclonus and angiokeratomas in adult galactosialidosis. Mov Disord. 26(4):756-7 [Download] [Pubmed]
Kauffman MA, Sterin-Prync A, Papouchado M, Gonzalez E, Vidal AJ, Grossberg SE, Chuppa S, Odoriz B, Vrech C, Diez RA, Ferro HH (2011). Immunogenicity of an interferon-beta1a product. Int J Immunopathol Pharmacol, 24(2):499-504 [Download] [Pubmed]
Kauffman MA, Gonzalez-Morón D, Garcea O, Villa AM (2011). TNFSFR1A R92Q mutation, autoinflammatory symptoms and multiple sclerosis in a cohort from Argentina. Mol Biol Rep. 39(1):117-21 [Download] [Pubmed]
Kauffman MA, Consalvo D, Gonzalez-Morón D, Pujol V, Kochen S (2010). ApoEε4 genotype and the age at onset of temporal lobe epilepsy: A case-control study and meta-analysis. Epilepsy Res, 90; 234-239 [Download] [Pubmed]
Gonzalez Morón D,Kauffman M, Garcea O, Villa AM (2010). Nuevos factores genéticos en la esclerosis múltiple: mutación R92Q en el gen TNFRSF1A y el síndrome autoinflamatorio TRAPS. Neurología Argentina 2; 29-34 [Download]
Kauffman MA, Consalvo D, Gonzalez-Morón D, Pujol V, Solís P, Oddo S, Lomlomdjian C, Kochen S (2009). El alelo e4 de la apolipoproteína e modificaría el “período silente” del desarrollo de la epilepsia mesial temporal con esclerosis del hipocampo. Neurología Argentina 1; 148-154 [Download]
Kauffman MA, Yankilevich P, Barrero P, Bello R, Marangunich L, Vidal A, Criscuolo M, Diez RA, SterinPrync A (2009). Whole genome analysis of the action of interferon-beta. Int J Clin PharmacolTher, 47; 328-57 [Download] [Pubmed]
Kauffman MA, Villa AM (2009). Comment to Tumour necrosis factor alpha gene -376 polymorphism in Hungarian patients with primary progressive multiple sclerosis. J Neuroimmunol, 212; 151 [Download] [Pubmed]
Kauffman MA, Consalvo D, Gonzalez-Morón D, Aguirre F, D'Alessio L, Kochen S (2009). Serotonin transporter gene variation and refractory mesial temporal epilepsy with hippocampal sclerosis. Epilepsy Res, 85; 231-234 [Download] [Pubmed]
Kauffman MA, Pereira-de-Silva N, Consalvo D, Kochen S (2009). ApoE epsilon4 is not associated with posictal confusion in patients with mesial temporal lobe epilepsy with hippocampal sclerosis. Epilepsy Res, 85; 311-313 [Download] [Pubmed]
Lahoz M, Kauffman M, Carfagnini J, Vidal A, Papouchado M, Sterin-Prync A, Diez R, Nagle C (2009). Pharmacokinetics and pharmacodynamics of interferon beta 1a in Cebus apella. J Med Primatol, 38; 187-191. [Download] [Pubmed]
D'Alessio L, Giagante B, Papayannis C, Oddo S, Silva W, Solís P, Donnoli V, Kauffman M, Consalvo D, Zieher LM, Kochen S (2009). Psychotic disorders in Argentine patients with refractory temporal lobe epilepsy: a case-control study. Epilepsy Behav, 14; 604-609 [Download] [Pubmed]
Melcon C, Consalvo D, Centurión E, Papayannis C, Kauffman M, Kochen S (2009). Heterotopía en banda o doble corteza. Reporte de caso. Neurología Argentina, 1; 47-49 [Download]
Arberas C, Aguirre F, Berardo A, GonzalezMoron D, Kauffman M, Maiola R, Melamud L, Pirra L, Seifer G (2008). Guías de Neurogenética de la Sociedad Neurológica Argentina. Rev Neurol Arg, 33; 86-94. [Download]
Kauffman M, Consalvo D, Gonzalez Morón D, Aguirre F, D´Alessio L, Kochen S (2008). Genotipificación del gen del recaptador de serotonina y respuesta al tratamiento en la epilepsia mesial temporal con esclerosis del hipocampo ¿pronóstico molecular?.Rev Neurol Arg, 33; 22-27. [Download]
Papayannis C, Consalvo D, Seifer G, Kauffman M, Silva W, Kochen S (2008). Clinical spectrum and difficulties in management of hypothalamic hamartoma in a developing country. Acta Neurol Scand,118: 313-19 [Download] [Pubmed]
Di Girolamo G, Kauffman M, Gonzalez E, Papouchado M, Ramírez A, Keller G, Carbonetto C, Dabsys S, Vidal A, Sterin-Prync A, Diez R (2008). Bioequivalence of Two Subcutaneous Pharmaceutical Products of Interferon Beta 1a. Drug Research, 58: 193-198 [Download] [Pubmed]
Kauffman M, Levy E, Consalvo D, Mordoh J, Kochen S (2008). GABABR1 (G1465A) gene variation and temporal lobe epilepsy controversy: new evidence. Seizure, 17; 567-71. [Download] [Pubmed]
Kauffman M, Consalvo D, Gonzalez Morón D, Kochen S (2008). Transcriptionally less active prodynorphin promoter alleles are associated with temporal lobe epilepsy: a case-control study and meta-analysis. Dis Markers, 24; 135-40. [Download] [Pubmed]
Kauffman M, Gonzalez Morón D, Consalvo D, Bello R, Kochen S (2008). Association study between interleukin 1β gene and epileptic disorders: a HuGe review and meta-analysis. Genetics in Medicine 10, 83-88. [Download] [Pubmed]
Prync AE, Yankilevich P, Barrero PR, Bello R, Marangunich L, Vidal A, Kauffman M, Diez RA (2008). Two recombinant human interferon-beta 1a pharmaceutical preparations produce a similar transcriptional response determined using whole genome microarrays analysis. Int J ClinPharmacolTher 46, 64-71 [Download] [Pubmed]
Kauffman M, Moron DG, Bruno V (2007). How accurate are bedside hearing test? Neurology 69 (13), 1382 [Download] [Pubmed]
Kauffman M, Gonzalez Morón D, Garcea O, Sica R, Villa AM (2007) Is tumour necrosis factor -376A promoter polymorphism associated with susceptibility to multiple sclerosis? Medicina (B Aires) 67 (5), 436-8. [Download] [Pubmed]
Kauffman M, Consalvo D, Kochen S. (2007) Genética de la Epilepsia del Lóbulo Temporal. Psicofarmacología, 7, 16-21. [Download]
Kauffman M, Consalvo D, GonzalezMoron D, Kochen S (2007) Asociación entre Alelos Transcripcionalmente Deficientes del gen de la Prodinorfina y el Desarrollo de Epilepsia del Lóbulo Temporal, Revista Neurológica Argentina, 32 (1), 40-46 [Download]
Kauffman M, Yankilevich P, Barrero P, SterynPrync A, Diez RA (2007) Caracterización de la expresión génica inducida por interferón beta en leucocitos de pacientes con Esclerosis Múltiple utilizando microarrays de genoma completo. Un Analisis Preliminar., Revista Neurológica Argentina, 32(2),105-117 [Download]
Kauffman M, Consalvo D, Levy E, Papayannis C, Mordoh J, Kochen S (2006) El Polimorfismo G1465A del Gen GABBR1 es un Marcador de Riesgo para el desarrollo de Epilepsia Mesial Temporal con Esclerosis del Hipocampo., Revista Neurológica Argentina, 31(1)25-31 [Download]
