Tatiéle Nalin - Concepedia

Author

Tatiéle Nalin

Universidade Federal do Rio Grande do Sul

Also Known As

Nalin, Tatiéle, Tatiele Nalin, Tatiéle Nalin

Publications

446

Citations

H-Index

Concepts

All Affiliations

Universidade Federal do Rio Grande do Sul Hospital de Clínicas de Porto Alegre University of Groningen Hospital Infantil Albert Sabin University Medical Center Groningen

About

Tatiéle Nalin is an author at Universidade Federal do Rio Grande do Sul specializing in urology, medicine, and health law.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	1	1	29
2	Health Law	1	1	29
3	Health Policy	1	1	29
4	Nephrology	1	1	29
5	Outcomes Research	1	1	29

Tatiéle Nalin

Publications

325

Citations

H-Index

Page 1

	Year	Citations
Maple syrup urine disease in Brazil: a panorama of the last two decades Silvani Herber, Ida Vanessa Döederlein Schwartz, Tatiéle Nalin, Jornal de Pediatria	2014	36
Glycogen storage disease type I: clinical and laboratory profile Berenice Lempek dos Santos, Carolina Fischinger Moura de Souza, Lavínia Schüler‐Faccini, Jornal de Pediatria	2014	35
Access to treatment for phenylketonuria by judicial means in Rio Grande do Sul, Brazil Luciano Mangueira Trevisan, Tatiéle Nalin, Tássia Tonon, Ciência & Saúde Coletiva UrologyHealth PolicyRio GrandeEvidence-based MedicineUnified Health System	2015	29
In vitro digestion of starches in a dynamic gastrointestinal model: an innovative study to optimize dietary management of patients with hepatic glycogen storage diseases Tatiéle Nalin, Koen Venema, David A. Weinstein, Journal of Inherited Metabolic Disease	2014	28
Hepatic glycogen storage diseases are associated to microbial dysbiosis Karina Colonetti, Bruna Bento dos Santos, Tatiéle Nalin, PLoS ONE	2019	28
Analysis of body composition and nutritional status in Brazilian phenylketonuria patients Priscila Nicolao Mazzola, Tatiéle Nalin, Kamila Castro, Molecular Genetics and Metabolism Reports	2016	25
Evaluation of the frequency of non-motor symptoms of Parkinson’s disease in adult patients with Gaucher disease type 1 Matheus Vernet Machado Bressan Wilke, Alícia Dorneles Dornelles, Artur Francisco Schumacher Schuh, Orphanet Journal of Rare Diseases	2019	22
Glycogen storage diseases: Twenty‐seven new variants in a cohort of 125 patients Fernanda Sperb‐Ludwig, Franciele Cabral Pinheiro, Malu Bettio Soares, Molecular Genetics & Genomic Medicine	2019	21
Food Neophobia in Patients With Phenylketonuria Tássia Tonon, Chenia Caldeira Martinez, Soraia Poloni, Journal of Endocrinology and Metabolism	2019	21
Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism Soraia Poloni, Sandra Leistner‐Segal, Isabel Cristina Bandeira, Gene	2014	20

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