Síndrome Hemolítico-Urêmica na infância

by Vaisbich,Maria Helena
Published 2014

Miosite e rabdomiólise na doença mão-pé-boca na infância

by Vaisbich,Maria Helena, Tozze,Roberto, Baldacci,Evandro Roberto
Published 2010

Pharmacokinetics of cyclosporin: a microemulsion in children with idiopathic nephrotic syndrome

by Henriques,Luciana dos Santos, Matos,Fabíola de Marcos, Vaisbich,Maria Helena
Published 2012

Treatment of Bartter syndrome. Unsolved issue,

by Nascimento,Carla Lessa Pena, Garcia,Cecilia Lopes, Schvartsman,Benita Galassi Soares, Vaisbich,Maria Helena
Published 2014

Marcadores práticos de função renal em pacientes com cistinose

by Guimaraes,Luciana Pache de Faria, Neri,Letícia Aparecida Lopes, Sumita,Nairo Massakasu, Vaisbich,Maria Helena
Published 2012

Dental abnormalities and oral health in patients with Hypophosphatemic rickets

by Souza,Melissa Almeida, Soares Junior,Luiz Alberto Valente, Santos,Marcela Alves dos, Vaisbich,Maria Helena
Published 2010

The long-term use of enalapril and hydrochlorothiazide in two novel mutations patients with Dent's disease type 1

by Vaisbich,Maria Helena, Henriques,Luciana dos Santos, Igarashi,Takashi, Sekine,Takashi, Seki,George, Koch,Vera H
Published 2012

Brazilian consensus recommendations for the diagnosis, screening, and treatment of individuals with fabry disease: Committee for Rare Diseases - Brazilian Society of Nephrology/202...

by Silva,Cassiano Augusto Braga, Andrade,Luis Gustavo Modelli de, Vaisbich,Maria Helena, Barreto,Fellype de Carvalho
Published 2022

Recommendations for the diagnosis and management of Fabry disease in pediatric patients: a document from the Rare Diseases Committee of the Brazilian Society of Nephrology (Comdora...

by Vaisbich,Maria Helena, Andrade,Luís Gustavo Modelli de, Silva,Cassiano Augusto Braga, Barreto,Fellype de Carvalho
Published 2022

Nephrogenic diabetes insipidus (NDI): clinical, laboratory and genetic characterization of five Brazilian patients

by Vaisbich,Maria Helena, Carneiro,Juliana, Bóson,Wolfanga, Resende,Bruna, De Marco,Luiz, Honjo,Rachel S, Kim,Chong Ae, Koch,Vera H
Published 2009

Fístula gastrocólica na síndrome de Bartter em uso de indometacina: relato de dois casos

by Barbosa,Priscila Rodrigues, Abe,Julie Mari, Oliveira,Luiz Antônio Nunes de, Vaisbich,Maria Helena, Koch,Vera H. K., Cerri,Giovanni Guido
Published 2003

Multidisciplinary approach for patients with nephropathic cystinosis: model for care in a rare and chronic renal disease

by Vaisbich,Maria Helena, Satiro,Carla Aline Fernandes, Roz,Deborah, Nunes,Debora de Almeida Domingues, Messa,Ana Carola H Lobo, Lanetzki,Camila, Ferreira,Juliana Caires de Oliveira Achili
Published 2019

COMDORA-SBN recommendations for patients with rare kidney diseases in relation to the Covid-19 pandemic

by Colares,Vinícius Sardão, Miranda,Silvana Maria, Andrade,Luis Gustavo Modelli de, Palma,Lilian Monteiro Pereira, Castro,Maria Cristina Ribeiro de, Silva,Cassiano Augusto Braga, Penido,Maria Goretti Moreira Guimarães, Sobral,Roberta, Vaisbich,Maria Helena
Published 2020

Uso do eculizumab na síndrome hemolítica urêmica atípica: relato de caso e revisão da literatura

by Vaisbich,Maria Helena, Henriques,Luciana dos Santos, Watanabe,Andréia, Pereira,Lilian Monteiro, Metran,Camila Cardoso, Malheiros,Denise Avancini, Modanez,Flávia, Silva,João Domingos Montoni da, Vieira,Simone, Macedo,Ana Catarina Lunz, Massarope,Bianca, Furusawa,Érika Arai, Schvartsman,Benita Galassi Soares
Published 2013