Norberto Guelbert

1.3k citations

39 papers · 651 indexed · h-index 16

Impact in

Physiology top 5%
- Lysosomal Storage Disorders Research
Rheumatology top 5%
- Glycogen Storage Diseases and Myoclonus

Papers in

Physiology 29
- Lysosomal Storage Disorders Research 29
Rheumatology 12
- Glycogen Storage Diseases and Myoclonus 12

Co-authors: Raquel Dodelson de Kremer Roberto Giugliani John J. Mitchell Barbara K. Burton Rossella Parini Christian J. Hendriksz Paul Harmatz Ana María Martins
Journals: Molecular Genetics and Metabolism (9 papers)Journal of Inherited Metabolic Disease (2 papers)Orphanet Journal of Rare Diseases (2 papers)Journal of Pain and Symptom Management (2 papers)Gene (1 paper)
Partner nations: Argentina United States Brazil

In The Last Decade

Norberto Guelbert

38 papers receiving 644 citations

Peers

Countries citing papers authored by Norberto Guelbert

Since Specialization

Citations

This map shows the geographic impact of Norberto Guelbert's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Norberto Guelbert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Norberto Guelbert more than expected).

Fields of papers citing papers by Norberto Guelbert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Norberto Guelbert. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Norberto Guelbert. The network helps show where Norberto Guelbert may publish in the future.

Co-authors

The 25 scholars most cited alongside Norberto Guelbert, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Norberto Guelbert Line = papers co-authored together Norberto Guelbert links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	“Atypical” Phenotypes of Neuronal Ceroid Lipofuscinosis: The Argentine Experience in the Genomic Era SHILAP Revista de lepidopterología ·菊地原靖孝, 啓太加藤, François Traincart, Peter Bentzen, R.Valigi Rvaligi, Hanna Källebo Neikter, Elmer A. Fernández, Ana Lucía De Paul, Norberto Guelbert, Kazufusa Sasahara	2021	1
2	Management of CLN1 Disease: International Clinical Consensus Pediatric Neurology ·Erika F. Augustine, Heather Adams, Emily de los Reyes, R Suzan Sanavi, Yaomal wahyu, Norberto Guelbert, Minna Laine, Pracha Yeunyongkul, Jonathan W. Mink, Miriam Nickel, Chandani Thakur, Angela Schulz, Alessandro Simonati, Meral Topçu, Joni A. Turunen, Ruth Williams, Elaine Wirrell, Jason Tremblay	2021	17
3	Cerliponase Alfa for the Treatment of Atypical Phenotypes of CLN2 Disease: A Retrospective Case Series Journal of Child Neurology ·Protik Mazumder, Raymond Wang, Emily de los Reyes, Nicola Specchio, Paul Gissen, Norberto Guelbert, Miriam Nickel, Yusufjon Mizomov, Lenora Lehwald, Marina Trivisano, Laura Lee, Wei Baotao, Jessica Cohen‐Pfeffer, Renée Shediac, Oliver Schips, Angela Schulz	2020	10
4	Position of Experts Regarding Follow-Up of Patients with Neuronal Ceroid Lipofuscinosis-2 Disease in Latin America SHILAP Revista de lepidopterología ·Norberto Guelbert, P. Djudovic, K. G. Trobeck, Kiri Koshu, 浦上慎司, 蔡艺榕, André Luiz Santos Pessoa, Norma Spécola, Constance Osafo-Adjei, M. Troncoso, 卢功志	2020	1
5	Urea cycle disorders in Argentine patients: clinical presentation, biochemical and genetic findings Orphanet Journal of Rare Diseases ·Changwen Wei, José Antonio Arranz, Johannes Häberle, André Santos da Rocha, Jesús Ramón Escajadillo, Norberto Guelbert, R.Valigi Rvaligi, VAN DER STRAETEN C, Raquel Dodelson de Kremer, Laura E. Laróvere	2019	5
6	Recommendations for Evaluation and Management of Pain in Patients With Mucopolysaccharidosis in Latin America Journal of Pain and Symptom Management ·Juan Politei, Shen Hai, Norberto Guelbert, Carolina Fischinger Moura de Souza, Charles Marques Lourenço, Laifa Kong, Bertil Malmberg, Fufung Setiawan, Ana María Martins	2018	5
7	Ten years of screening for congenital disorders of glycosylation in Argentina: case studies and pitfalls Pediatric Research ·Carla Asteggiano, Alervo Saarikoski, Antonio Sánchez Ruiz, Devendra Reddy Rachapalli, Bill Jaspersohn, 覃玉欧, Norberto Guelbert, Ana Elena Escalante Hernández, 박일룡, Raquel Dodelson de Kremer	2018	18
8	Impact of long-term elosulfase alfa on activities of daily living in patients with Morquio A syndrome in an open-label, multi-center, phase 3 extension study Molecular Genetics and Metabolism ·Christian J. Hendriksz, Rossella Parini, Moeenaldeen AlSayed, Julian Raiman, Roberto Giugliani, John J. Mitchell, Barbara K. Burton, Norberto Guelbert, Fiona Stewart, Derralynn Hughes, Robert Matousek, Sara M. Hawley, Celeste Decker, Paul Harmatz	2017	22
9	Long-term endurance and safety of elosulfase alfa enzyme replacement therapy in patients with Morquio A syndrome Molecular Genetics and Metabolism ·Christian J. Hendriksz, Rossella Parini, Moeenaldeen AlSayed, Julian Raiman, Roberto Giugliani, Rajkinkar Chakraborty, John J. Mitchell, Barbara K. Burton, Norberto Guelbert, Fiona Stewart, Derralynn Hughes, Kenneth I. Berger, Peter Slasor, Robert Matousek, Elaina Jurecki, Adam J. Shaywitz, Paul Harmatz	2016	50
10	Enfermedad de Morquio (mucopolisacaridosis IV-A): aspectos clínicos, diagnósticos y nuevo tratamiento con terapia de reemplazo enzimático Archivos Argentinos de Pediatria ·Juan Politei, Andrea Schenone, Norberto Guelbert, Ababaikere HALIKE, Marina Szlago	2015	7
11	The neuronal ceroid lipofuscinoses program: A translational research experience in Argentina Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·KrishanL Chachra, 菊地原靖孝, Norberto Guelbert, Patricia Pons, Bartłomiej Krawczyk, Xiaochuan Yu, R.Valigi Rvaligi, Katherine B. Sims, Winnie Xin, Peter Bentzen, Inés Noher de Halac	2015	18
12	Early treatment with laronidase improves clinical outcomes in patients with attenuated MPS I: a retrospective case series analysis of nine sibships Orphanet Journal of Rare Diseases ·Nouriya Al‐Sannaa, Lodovico Riva di Sanseverino, Deborah Barbouth, Hui Ren, Cyril Goizet, Norberto Guelbert, Simon Jones, Sandra Obikawa Kyosen, Ana María Martins, Chanika Phornphutkul, Seung-Pyo Lee, Joris Michiels, Shari Fallet, Krista Lamb	2015	60
13	SAT0493 Farber Disease: First Natural History Cohort Demonstrates a Broad Clinical Spectrum with Implications for Juvenile Idiopathic Arthritis Patients Annals of the Rheumatic Diseases ·Amy Waren, Karoline Ehlert, Boris Hügle, Bo Magnusson, Giedré Grigelioniené, Norberto Guelbert, Janet Gardner‐Medwin, Pranoot Tanpaiboon, Lawrence Jung, Ratna Dua Puri, M. DiRocco, John J. Mitchell, Martín Beck, Calogera M. Simonaro, Edward H. Schuchman	2015	1
14	Longitudinal analysis of endurance and respiratory function from a natural history study of Morquio A syndrome Molecular Genetics and Metabolism ·Paul Harmatz, Eugen Mengel, Roberto Giugliani, Vassili Valayannopoulos, Shuan-Pei Lin, Rossella Parini, Nathalie Guffon, Barbara K. Burton, Christian J. Hendriksz, John J. Mitchell, Ana María Martins, Simon Jones, Norberto Guelbert, Ashok Vellodi, Frits A. Wijburg, Kehu Yang, Peter Slasor, Celeste Decker	2014	31
15	The Morquio A Clinical Assessment Program: Baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects Molecular Genetics and Metabolism ·Paul Harmatz, Eugen Mengel, Roberto Giugliani, Vassili Valayannopoulos, Shuan-Pei Lin, Rossella Parini, Nathalie Guffon, Barbara K. Burton, Christian J. Hendriksz, John J. Mitchell, Ana María Martins, Simon Jones, Norberto Guelbert, Ashok Vellodi, Carla E. M. Hollak, Peter Slasor, Celeste Decker	2013	110
16	Neuronal ceroid lipofuscinosis type CLN2: A new rationale for the construction of phenotypic subgroups based on a survey of 25 cases in South America Gene ·KrishanL Chachra, R. Schneppenheim, Winnie Xin, Katherine B. Sims, Norberto Guelbert, Peter Bentzen, Patricia Pons, Mateng Si, M. Troncoso, Agra Utari Dewi, David A. Pearce, Raquel Dodelson de Kremer, Bartłomiej Krawczyk, Inés Noher de Halac	2012	34
17	Therapeutic Approaches to the Challenge of Neuronal Ceroid Lipofuscinoses Current Pharmaceutical Biotechnology ·KrishanL Chachra, Peter Bentzen, Bartłomiej Krawczyk, Norberto Guelbert, Gláudia Maria Bovi Ambrosano, Mateng Si, Sara Mole, Raquel Dodelson de Kremer, Inés Noher de Halac	2011	40
18	Two Argentinean Siblings with CDG-Ix: A Novel Type of Congenital Disorder of Glycosylation? JIMD Reports ·Antonio Sánchez Ruiz, Asmaa Amin Abdelaziz, Bill Jaspersohn, Norberto Guelbert, Luisa Sturiale, Domenico Garozzo, Gert Matthijs, J. Jaeken, Raquel Dodelson de Kremer, Carla Asteggiano	2011	6
19	An integrated strategy for the diagnosis of neuronal ceroid lipofuscinosis types 1 (CLN1) and 2 (CLN2) in eleven Latin American patients Clinical Genetics ·KrishanL Chachra, Tan Haili, Raquel Dodelson de Kremer, Amin Shafiei, Norberto Guelbert, Gláudia Maria Bovi Ambrosano, Pietro. Fanfani, MLE Andersson, Inés Noher de Halac	2009	22
20	Identification of a common mutation in mucopolysaccharidosis IVA: correlation among genotype, phenotype, and keratan sulfate Journal of Human Genetics ·Shunji Tomatsu, می فؤاد الغویط, Ida Vanessa Döederlein Schwartz, Ba Yanheshig, Roberto Giugliani, Luis A. Barrera, Norberto Guelbert, Raquel Dodelson de Kremer, Gabriela M. Repetto, Mónica Gutiérrez, Tatsuo Nishioka, Saad Nader, Adriana M. Montaño, Seiji Yamaguchi, Akihiko Noguchi	2004	39

About Norberto Guelbert

Norberto Guelbert is a scholar working on Physiology, Rheumatology, Cell Biology, Clinical Biochemistry and Epidemiology, having authored 39 papers that have together received 651 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (29 papers), Glycogen Storage Diseases and Myoclonus (12 papers), Trypanosoma species research and implications (10 papers), Cellular transport and secretion (6 papers), Biochemical and Molecular Research (4 papers), Glycosylation and Glycoproteins Research (3 papers), Child Nutrition and Feeding Issues (3 papers) and Metabolism and Genetic Disorders (3 papers). The work is most often cited by research in Physiology (514 citations), Rheumatology (232 citations), Clinical Biochemistry (48 citations), Cell Biology (105 citations) and Epidemiology (216 citations). Norberto Guelbert has collaborated with scholars based in Argentina, United States and Brazil. Frequent co-authors include Raquel Dodelson de Kremer, Roberto Giugliani, John J. Mitchell, Barbara K. Burton, Rossella Parini, Christian J. Hendriksz, Paul Harmatz, Ana María Martins, Simon Jones and Inés Noher de Halac. Their work appears in journals such as Molecular Genetics and Metabolism, Journal of Inherited Metabolic Disease, Orphanet Journal of Rare Diseases, Journal of Pain and Symptom Management and Gene.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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