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Doederlein-Schwartz, Ida Vanessa
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1

Editorial: Inborn errors of carbohydrate metabolism:

Martínez-Duncker, Iván ; Doederlein-Schwartz, Ida Vanessa ; Abreu-González, Melania.
Frontiers in Genetics.  15 (2024)  - p. , 2024
Link: https://doi.org/10.3389/..
 
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Cytokine profiling in patients with hepatic glycogen storag..:

Colonetti, Karina ; Pinto e Vairo, Filippo ; Siebert, Marina...
Cytokine.  162 (2023)  - p. 156088 , 2023
Link: https://doi.org/10.1016/..
 
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3

Correction: Hepatic glycogen storage diseases are associate..:

Colonetti, Karina ; Bento dos Santos, Bruna ; Nalin, Tatiéle...
PLOS ONE.  14 (2019)  6 - p. e0218254 , 2019
Link: https://doi.org/10.1371/..
 
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4

Brain-derived neurotrophic factor expression increases afte..:

Vairo, Filippo ; Sperb-Ludwig, Fernanda ; Wilke, Matheus...
Journal of Neuroimmunology.  278 (2015)  - p. 190-193 , 2015
Link: https://doi.org/10.1016/..
 
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5

Visual Dysfunction of Type I and VI Mucopolysaccharidosis P..:

Duarte Gomes, Bruno ; da Silva Souza, Givago ; Monteiro Viana, Gustavo...
Case Reports in Ophthalmology.  3 (2012)  1 - p. 104-112 , 2012
Link: https://doi.org/10.1159/..
 
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6

Mortality profile in a cohort of patients with Gaucher dise..:

Teixeira, Lucas ; Randon, Devora ; Poswar, Fabiano.
Molecular Genetics and Metabolism.  141 (2024)  4 - p. 108265 , 2024
Link: https://doi.org/10.1016/..
 
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7

Identification of metabolic pathways and key genes associat..:

Pasqualotto, Amanda ; da Silva, Vinícius ; Pellenz, Felipe Mateus...
Metabolic Brain Disease.  39 (2024)  4 - p. 577-587 , 2024
Link: https://doi.org/10.1007/..
 
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8

Adherence to PKU guidelines among patients with phenylketon..:

Chiesa, Ana ; Spécola, Norma ; Poubel, Monique...
Molecular Genetics and Metabolism Reports.  38 (2024)  - p. 101026 , 2024
Link: https://doi.org/10.1016/..
 
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9

General overview of urea cycle disorders (UCDs) in Brazil:

Schwartz, Ida Vanessa Doederlein ; dos Santos, Mariana Lopes ; Fink, Isabela Alicia...
Molecular Genetics and Metabolism.  141 (2024)  4 - p. 108217 , 2024
Link: https://doi.org/10.1016/..
 
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10

An adult with cystathionine beta-synthase deficiency, campt..:

Donis, Karina Carvalho ; Kalil, Marco Antônio Baptista ; Poswar, Fabiano...
Genetics and Molecular Biology.  47 (2024)  1 - p. , 2024
Link: https://doi.org/10.1590/..
 
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11

Brazilian cohort of patients diagnosed with glucose transpo..:

Sobrinho, Livia ; Refosco, Lilia ; Poswar, Fabiano..
Molecular Genetics and Metabolism.  141 (2024)  4 - p. 108261 , 2024
Link: https://doi.org/10.1016/..
 
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12

Rare diseases diagnosed through neonatal screening: Data fr..:

Milke, Júlia Cordeiro ; de Oliveira, Bibiana Mello ; Schmidt, Amanda Maria...
Molecular Genetics and Metabolism.  141 (2024)  4 - p. 108337 , 2024
Link: https://doi.org/10.1016/..
 
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13

Homocysteine and methylmalonic acid in Phenylketonuria pati..:

Hoss, Giovana Regina Weber ; Sperb-Ludwig, Fernanda ; Tonon, Tássia...
Genetics and Molecular Biology.  46 (2023)  3 suppl 1 - p. , 2023
Link: https://doi.org/10.1590/..
 
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14

Feeding difficulties in patients with Phenylketonuria:

Rocha, Alexia Diovana Fernandes da ; Martinez, Chenia Caldeira ; Refosco, Lilia Farret...
CoDAS.  35 (2023)  6 - p. , 2023
Link: https://doi.org/10.1590/..
 
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15

GENOME SEQUENCING FOR PATIENTS WITH SUSPECTED INHERITED MET..:

Schwartz, Ida Vanessa Doederlein ; Silva, Thiago Oliveira ; Poswar, Fabiano...
Molecular Genetics and Metabolism.  138 (2023)  3 - p. 107405 , 2023
Link: https://doi.org/10.1016/..
 
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