Следене
Sandra Leistner-Segal
Sandra Leistner-Segal
Hospital de Clínicas de Porto Alegre/Medical Genetics Service/Molecular Genetics Laboratory
Потвърден имейл адрес: hcpa.edu.br
Заглавие
Позовавания
Позовавания
Година
A clinical study of 77 patients with mucopolysaccharidosis type II
IVD Schwartz, MG Ribeiro, JG Mota, MBP Toralles, P Correia, D Horovitz, ...
Acta Paediatrica 96, 63-70, 2007
1722007
Hematopoietic stem cell transplantation for patients with mucopolysaccharidosis II
F Kubaski, H Yabe, Y Suzuki, T Seto, T Hamazaki, RW Mason, L Xie, ...
Biology of Blood and Marrow Transplantation 23 (10), 1795-1803, 2017
922017
Lack of association between the Serotonin Transporter Promoter Polymorphism (5-HTTLPR) and Panic Disorder: a systematic review and meta-analysis
C Blaya, GA Salum, MS Lima, S Leistner-Segal, GG Manfro
Behavioral and brain functions 3, 1-10, 2007
902007
Detection of human bocavirus and human metapneumovirus by real-time PCR from patients with respiratory symptoms in Southern Brazil
DA Pilger, VV Cantarelli, SL Amantea, S Leistner-Segal
Memorias do Instituto Oswaldo Cruz 106, 56-60, 2011
822011
Diagnostic and treatment strategies in mucopolysaccharidosis VI
F Vairo, A Federhen, G Baldo, M Riegel, M Burin, S Leistner-Segal, ...
The application of clinical genetics, 245-255, 2015
742015
The BDNF Val66Met polymorphism is an independent risk factor for high lethality in suicide attempts of depressed patients
LC Schenkel, J Segal, JA Becker, GG Manfro, MM Bianchin, ...
Progress in Neuro-Psychopharmacology and Biological Psychiatry 34 (6), 940-944, 2010
692010
The multidimensional evaluation and treatment of anxiety in children and adolescents: rationale, design, methods and preliminary findings
GA Salum, LR Isolan, VL Bosa, AG Tocchetto, SP Teche, I Schuch, ...
Brazilian Journal of Psychiatry 33, 181-195, 2011
682011
Diagnosis of mucopolysaccharidoses
F Kubaski, F de Oliveira Poswar, K Michelin-Tirelli, MG Burin, ...
Diagnostics 10 (3), 172, 2020
602020
Molecular testing of 163 patients with Morquio A (Mucopolysaccharidosis IVA) identifies 39 novel GALNS mutations
A Morrone, KL Tylee, M Al-Sayed, AC Brusius-Facchin, A Caciotti, ...
Molecular Genetics and Metabolism 112 (2), 160-170, 2014
592014
Mucopolysaccharidosis type II: identification of 30 novel mutations among Latin American patients
AC Brusius-Facchin, IVD Schwartz, C Zimmer, MG Ribeiro, AX Acosta, ...
Molecular genetics and metabolism 111 (2), 133-138, 2014
522014
Panic disorder and serotonergic genes (SLC6A4, HTR1A and HTR2A): association and interaction with childhood trauma and parenting
C Blaya, GA Salum, P Moorjani, AC Seganfredo, E Heldt, ...
Neuroscience letters 485 (1), 11-15, 2010
522010
Genetic studies in a cluster of mucopolysaccharidosis type VI patients in Northeast Brazil
FM Costa-Motta, AX Acosta, K Abé-Sandes, F Bender, IVD Schwartz, ...
Molecular Genetics and Metabolism 104 (4), 603-607, 2011
512011
Intellectual disability in a birth cohort: prevalence, etiology, and determinants at the age of 4 years
SM Karam, AJD Barros, A Matijasevich, IS Dos Santos, L Anselmi, ...
Public Health Genomics 19 (5), 290-297, 2016
492016
A community-based study of mucopolysaccharidosis type VI in Brazil: the influence of founder effect, endogamy and consanguinity
FM Costa-Motta, F Bender, A Acosta, K Abé-Sandes, T Machado, ...
Human heredity 77 (1-4), 189-196, 2014
462014
Mucopolysaccharidosis type VI: Identification of novel mutations on the arylsulphatase B gene in South American patients
MFG Petry, K Nonemacher, JC Sebben, IVD Schwartz, ACM Azevedo, ...
Journal of inherited metabolic disease 28, 1027-1034, 2005
442005
Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil
CV Dillenburg, IC Bandeira, TV Tubino, LG Rossato, ES Dias, ...
Genetics and molecular biology 35, 599-602, 2012
432012
Analysis of KIR gene frequencies and HLA class I genotypes in breast cancer and control group
MR Jobim, M Jobim, PH Salim, P Portela, LF Jobim, S Leistner-Segal, ...
Human Immunology 74 (9), 1130-1133, 2013
402013
Serotonin transporter gene (5HTT) polymorphisms and temporal lobe epilepsy
LC Schenkel, JA Bragatti, CM Torres, KC Martin, G Gus-Manfro, ...
Epilepsy research 95 (1-2), 152-157, 2011
392011
Identification of β thalassemia mutations in South Brazilians
VCD Reichert, SM De Castro, SC Wagner, DM De Albuquerque, MH Hutz, ...
Annals of Hematology 87, 381-384, 2008
382008
Serotonin gene polymorphisms and psychiatry comorbidities in temporal lobe epilepsy
LC Schenkel, JA Bragatti, JA Becker, CM Torres, KC Martin, AC de Souza, ...
Epilepsy research 99 (3), 260-266, 2012
372012
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Статии 1–20