Dafne Dain Gandelman Horovitz

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 9

Top Topics

Bone Regeneration

Top Venues

Children (Basel, Switzerland)

Cadernos de saude publica

This page only lists publications with an associated author ORCID identifier.

Publications

Ana Paula Corrêa Cabral, Dafne Dain Gandelman Horovitz, Lidiane Nogueira Santos, Amanda Oliveira de Carvalho, Cristina Maria Duarte Wigg, Luciana Castaneda, Liane Simon, Carla Trevisan Martins Ribeiro
The 22q11.2 Deletion Syndrome from A Biopsychosocial Perspective: A Series of Cases with an ICF-Based Approach. Children (Basel, Switzerland) 11 (7) (2024)
Ana Paula Corrêa Cabral, Dafne Dain Gandelman Horovitz, Lidiane Nogueira Santos, Amanda Oliveira de Carvalho, Cristina Maria Duarte Wigg, Luciana Castaneda, Liane Simon, Carla Trevisan Martins Ribeiro
The 22q11.2 Deletion Syndrome from A Biopsychosocial Perspective: A Series of Cases with an ICF-Based Approach. Children (Basel, Switzerland) 11 (7) (2024)
Ana Paula Corrêa Cabral, Dafne Dain Gandelman Horovitz, Lidiane Nogueira Santos, Amanda Oliveira de Carvalho, Cristina Maria Duarte Wigg, Luciana Castaneda, Liane Simon, Carla Trevisan Martins Ribeiro
The 22q11.2 Deletion Syndrome from A Biopsychosocial Perspective: A Series of Cases with an ICF-Based Approach. Children (Basel, Switzerland) 11 (7) (2024)
Dafne Dain Gandelman Horovitz, Têmis Maria Félix, Victor Evangelista de Faria Ferraz
Medical Genetics in Brazil in the 21st Century: A Thriving Specialty and Its Incorporation in Public Health Policies. Genes 15 (8) (2024)
Dafne Dain Gandelman Horovitz, Têmis Maria Félix, Victor Evangelista de Faria Ferraz
Medical Genetics in Brazil in the 21st Century: A Thriving Specialty and Its Incorporation in Public Health Policies. Genes 15 (8) (2024)
Juliana Alves Josahkian, Ana Carolina Brusius Facchin, Alice Brinckmann Oliveira Netto, Sandra Leistner-Segal, Diana Rojas Málaga, Maira Graeff Burin, Kristiane Michelin-Tirelli, Franciele Barbosa Trapp, Augusto César Cardoso Dos Santos, Erlane Marques Ribeiro, Chong Ae Kim, Ana Cecília Menezes de Siqueira, Mara Lucia Schmitz Ferreira Santos, Daniel Almeida do Valle, Raquel Tavares Boy da Silva, Dafne Dain Gandelman Horovitz, Paula Frassinetti Vasconcelos de Medeiros, Carolina Fischinger Moura de Souza, Liane de Rosso Giuliani, Diego Santana Chaves Geraldo Miguel, Luiz Carlos Santana da Silva, Marcial Francis Galera, Roberto Giugliani
Genotype-phenotype studies in a large cohort of Brazilian patients with Hunter syndrome. American journal of medical genetics. Part C, Seminars in medical genetics 187 (3) (2021)
Ana Paula Carvalho Corrêa, Carla Trevisan Martins Ribeiro, Dafne Dain Gandelman Horovitz, Luciana Castaneda Ribeiro
Identification of relevant International Classification of Functioning Disability and Health (ICF) categories in patients with 22q11.2 Deletion Syndrome: a Delphi exercise. CoDAS 32 (6) (2020)
Martha Cristina Nunes Moreira, Marcos Antonio Ferreira do Nascimento, Daniel de Souza Campos, Lidianne Albernaz, Ana Carolina Carioca da Costa, Letícia Baptista de Paula Barros, Dafne Dain Gandelman Horovitz, Antilia Januária Martins, Adelino Furtado Madureira, Nicole Velloso de Oliveira, Marcia Ferreira Teixeira Pinto
Rare diseases and the associative dialogue: resignifications for moral experiences. Ciencia & saude coletiva 24 (10) (2019)
Marcia Ferreira Teixeira Pinto, Adelino Furtado Madureira, Letícia Baptista de Paula Barros, Marcos Antonio Ferreira do Nascimento, Ana Carolina Carioca da Costa, Nicole Velloso de Oliveira, Lidianne Albernaz, Daniel de Souza Campos, Dafne Dain Gandelman Horovitz, Antilia Januária Martins, Martha Cristina Nunes Moreira
[Complex care, high cost, and loss of income: frequent issues for families of children and adolescents with rare health conditions]. Cadernos de saude publica 35 (9) (2019)