Author Search Results

1

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

by Vaisbich,Maria Helena

Published 2010

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2

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

by Vaisbich,Maria Helena

Published 2012

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3

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

by Vaisbich,Maria Helena

Published 2013

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4

Síndrome Hemolítico-Urêmica na infância

by Vaisbich,Maria Helena

Published 2014

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5

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

Published 2022

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6

Baseline characteristics and evolution of Brazilian patients with atypical hemolytic uremic syndrome: first report of the Brazilian aHUS Registry

by Vaisbich, Maria Helena

Published 2022

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7

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

Published 2022

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8

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

by Vaisbich, Maria Helena

Published 2009

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9

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

by Henriques, Luciana dos Santos

Published 2012

Other Authors: “...Vaisbich, Maria Helena...”
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10

Marcadores práticos de função renal em pacientes com cistinose

by Guimaraes,Luciana Pache de Faria

Published 2012

Other Authors: “...Vaisbich,Maria Helena...”
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11

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

Published 2022

Other Authors: “...Vaisbich,Maria Helena...”
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12

Treatment of Bartter syndrome. Unsolved issue,

by Nascimento,Carla Lessa Pena

Published 2014

Other Authors: “...Vaisbich,Maria Helena...”
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13

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

Published 2022

Other Authors: “...Vaisbich, Maria Helena...”
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14

Dental abnormalities and oral health in patients with Hypophosphatemic rickets

by Souza, Melissa Almeida

Published 2010

Other Authors: “...Vaisbich, Maria Helena...”
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15

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

by Barbosa,Priscila Rodrigues

Published 2003

Other Authors: “...Vaisbich,Maria Helena...”
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16

Clinical and diagnostic aspects of Fabry disease management : a narrative review with a particular focus on Brazilian experts’ perspectives

by Giugliani, Roberto

Published 2021

Other Authors: “...Vaisbich, Maria Helena...”
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17

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

by Colares,Vinícius Sardão

Published 2020

Other Authors: “...Vaisbich,Maria Helena...”
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18

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

by Colares, Vinícius Sardão

Published 2020

Other Authors: “...Vaisbich, Maria Helena...”
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19

Eculizumab interruption in atypical hemolytic uremic syndrome due to shortage: analysis of a Brazilian cohort

by Neto, Miguel Ernandes [UNESP]

Published 2021

Other Authors: “...Vaisbich, Maria Helena...”
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20

ATYPICAL HEMOLYTIC UREMIC SYNDROME RELAPSE AFTER UNPLANNED ECULIZUMAB THERAPY DISCONTINUATION: RESULTS OF A BRAZILIAN SHORTAGE

by Neto, Miguel Ernandes

Published 2019

Other Authors: “...Vaisbich, Maria Helena...”
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