OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Proposal for a simplified classification of IMD based on a pathophysiological approach: A practical guide for clinicians
Jean‐Marie Saudubray, Fanny Mochel, Foudil Lamari, et al.
Journal of Inherited Metabolic Disease (2019) Vol. 42, Iss. 4, pp. 706-727
Closed Access | Times Cited: 54
Jean‐Marie Saudubray, Fanny Mochel, Foudil Lamari, et al.
Journal of Inherited Metabolic Disease (2019) Vol. 42, Iss. 4, pp. 706-727
Closed Access | Times Cited: 54
Showing 1-25 of 54 citing articles:
An international classification of inherited metabolic disorders (ICIMD )
Carlos R. Ferreira, Shamima Rahman, Markus A. Keller, et al.
Journal of Inherited Metabolic Disease (2020) Vol. 44, Iss. 1, pp. 164-177
Open Access | Times Cited: 233
Carlos R. Ferreira, Shamima Rahman, Markus A. Keller, et al.
Journal of Inherited Metabolic Disease (2020) Vol. 44, Iss. 1, pp. 164-177
Open Access | Times Cited: 233
Genetic disorders of cellular trafficking
Ángeles García‐Cazorla, Alfonso Oyarzábal, Jean‐Marie Saudubray, et al.
Trends in Genetics (2022) Vol. 38, Iss. 7, pp. 724-751
Closed Access | Times Cited: 44
Ángeles García‐Cazorla, Alfonso Oyarzábal, Jean‐Marie Saudubray, et al.
Trends in Genetics (2022) Vol. 38, Iss. 7, pp. 724-751
Closed Access | Times Cited: 44
BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening
Trine Tangeraas, Juliana R Constante, Paul Hoff Backe, et al.
Brain (2023) Vol. 146, Iss. 7, pp. 3003-3013
Closed Access | Times Cited: 23
Trine Tangeraas, Juliana R Constante, Paul Hoff Backe, et al.
Brain (2023) Vol. 146, Iss. 7, pp. 3003-3013
Closed Access | Times Cited: 23
Energy metabolism in childhood neurodevelopmental disorders
Alfonso Oyarzábal, Uliana Musokhranova, Barros LF, et al.
EBioMedicine (2021) Vol. 69, pp. 103474-103474
Open Access | Times Cited: 50
Alfonso Oyarzábal, Uliana Musokhranova, Barros LF, et al.
EBioMedicine (2021) Vol. 69, pp. 103474-103474
Open Access | Times Cited: 50
Lipidomics—Paving the Road towards Better Insight and Precision Medicine in Rare Metabolic Diseases
Martina Zandl‐Lang, Barbara Plecko, Harald Köfeler
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 2, pp. 1709-1709
Open Access | Times Cited: 11
Martina Zandl‐Lang, Barbara Plecko, Harald Köfeler
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 2, pp. 1709-1709
Open Access | Times Cited: 11
Urgences métaboliques néonatales
F. Labarthe, Violette Goetz, Marion Tardieu
EMC - Pédiatrie - Maladies infectieuses (2025) Vol. 45, Iss. 1, pp. 1-11
Closed Access
F. Labarthe, Violette Goetz, Marion Tardieu
EMC - Pédiatrie - Maladies infectieuses (2025) Vol. 45, Iss. 1, pp. 1-11
Closed Access
“Trafficking Disorders: Phenotypical Similarities and Differences With Other IMDs ”
Àngels García‐Cazorla, Éva Morava, Jean‐Marie Saudubray
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
Àngels García‐Cazorla, Éva Morava, Jean‐Marie Saudubray
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
Immunization coverage and timeliness of vaccination in young patients with inborn errors of metabolism: a French multicentric study
Anne-Sophie Renous, Léna Damaj, Magali Gorce, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Anne-Sophie Renous, Léna Damaj, Magali Gorce, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Cardiac manifestations in adult patients with inherited metabolic disease: A single-center experience
Flutura Sadiku, Tobias Rutz, Andrea Superti‐Furga, et al.
Molecular Genetics and Metabolism Reports (2025) Vol. 43, pp. 101216-101216
Closed Access
Flutura Sadiku, Tobias Rutz, Andrea Superti‐Furga, et al.
Molecular Genetics and Metabolism Reports (2025) Vol. 43, pp. 101216-101216
Closed Access
SUDEP in inherited metabolic epilepsies
Itay Tokatly Latzer, Charity Adams, Gardiner Lapham, et al.
Epilepsy & Behavior (2025) Vol. 168, pp. 110422-110422
Closed Access
Itay Tokatly Latzer, Charity Adams, Gardiner Lapham, et al.
Epilepsy & Behavior (2025) Vol. 168, pp. 110422-110422
Closed Access
Inherited disorders of complex lipid metabolism: A clinical review
Changrui Xiao, Francis Rossignol, Frédéric M. Vaz, et al.
Journal of Inherited Metabolic Disease (2021) Vol. 44, Iss. 4, pp. 809-825
Closed Access | Times Cited: 24
Changrui Xiao, Francis Rossignol, Frédéric M. Vaz, et al.
Journal of Inherited Metabolic Disease (2021) Vol. 44, Iss. 4, pp. 809-825
Closed Access | Times Cited: 24
Metabolomic Studies in Inborn Errors of Metabolism: Last Years and Future Perspectives
Marcello Cossu, Roberta Pintus, Marco Zaffanello, et al.
Metabolites (2023) Vol. 13, Iss. 3, pp. 447-447
Open Access | Times Cited: 9
Marcello Cossu, Roberta Pintus, Marco Zaffanello, et al.
Metabolites (2023) Vol. 13, Iss. 3, pp. 447-447
Open Access | Times Cited: 9
Clinico-radiological phenotyping and diagnostic pathways in childhood neurometabolic disorders—a practical introductory guide
Asthik Biswas, Mukul Malhotra, Kshitij Mankad, et al.
Translational Pediatrics (2021) Vol. 10, Iss. 4, pp. 1201-1230
Open Access | Times Cited: 22
Asthik Biswas, Mukul Malhotra, Kshitij Mankad, et al.
Translational Pediatrics (2021) Vol. 10, Iss. 4, pp. 1201-1230
Open Access | Times Cited: 22
The landscape of CRISPR/Cas9 for inborn errors of metabolism
Andrés Felipe Leal, Nidhi Fnu, Eliana Benincore-Flórez, et al.
Molecular Genetics and Metabolism (2022) Vol. 138, Iss. 1, pp. 106968-106968
Open Access | Times Cited: 14
Andrés Felipe Leal, Nidhi Fnu, Eliana Benincore-Flórez, et al.
Molecular Genetics and Metabolism (2022) Vol. 138, Iss. 1, pp. 106968-106968
Open Access | Times Cited: 14
3D Printing of Dietary Products for the Management of Inborn Errors of Intermediary Metabolism in Pediatric Populations
Paola Carou‐Senra, Lucía Rodríguez‐Pombo, Einés Monteagudo-Vilavedra, et al.
Nutrients (2023) Vol. 16, Iss. 1, pp. 61-61
Open Access | Times Cited: 8
Paola Carou‐Senra, Lucía Rodríguez‐Pombo, Einés Monteagudo-Vilavedra, et al.
Nutrients (2023) Vol. 16, Iss. 1, pp. 61-61
Open Access | Times Cited: 8
A narrative review of metabolomics in the era of “-omics”: integration into clinical practice for inborn errors of metabolism
Ashley Hertzog, Arthavan Selvanathan, Beena Devanapalli, et al.
Translational Pediatrics (2022) Vol. 11, Iss. 10, pp. 1704-1716
Open Access | Times Cited: 13
Ashley Hertzog, Arthavan Selvanathan, Beena Devanapalli, et al.
Translational Pediatrics (2022) Vol. 11, Iss. 10, pp. 1704-1716
Open Access | Times Cited: 13
Clouds over IMD? Perspectives for inherited metabolic diseases in adults from a retrospective cohort study in two Swiss adult metabolic clinics
Karim Gariani, Marina Nascimento, Andrea Superti‐Furga, et al.
Orphanet Journal of Rare Diseases (2020) Vol. 15, Iss. 1
Open Access | Times Cited: 20
Karim Gariani, Marina Nascimento, Andrea Superti‐Furga, et al.
Orphanet Journal of Rare Diseases (2020) Vol. 15, Iss. 1
Open Access | Times Cited: 20
The interplay between glucose and ketone bodies in neural stem cell metabolism
Joseph W. Molloy, Denis Barry
Journal of Neuroscience Research (2024) Vol. 102, Iss. 5
Closed Access | Times Cited: 2
Joseph W. Molloy, Denis Barry
Journal of Neuroscience Research (2024) Vol. 102, Iss. 5
Closed Access | Times Cited: 2
Movement Disorders and Liver Disease
Eoin Mulroy, Francesca Baschieri, Francesca Magrinelli, et al.
Movement Disorders Clinical Practice (2021) Vol. 8, Iss. 6, pp. 828-842
Open Access | Times Cited: 15
Eoin Mulroy, Francesca Baschieri, Francesca Magrinelli, et al.
Movement Disorders Clinical Practice (2021) Vol. 8, Iss. 6, pp. 828-842
Open Access | Times Cited: 15
Laboratory Diagnosis of Lysosomal Diseases: Newborn Screening to Treatment
Maria Fuller
Clinical biochemist reviews (2020) Vol. 41, Iss. 2
Open Access | Times Cited: 15
Maria Fuller
Clinical biochemist reviews (2020) Vol. 41, Iss. 2
Open Access | Times Cited: 15
Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomalies
Stephanie Allen, Natalie Chandler, Esther Kinning, et al.
Prenatal Diagnosis (2023) Vol. 44, Iss. 4, pp. 432-442
Closed Access | Times Cited: 5
Stephanie Allen, Natalie Chandler, Esther Kinning, et al.
Prenatal Diagnosis (2023) Vol. 44, Iss. 4, pp. 432-442
Closed Access | Times Cited: 5
Brève histoire des maladies métaboliques héréditaires
Jean‐Marie Saudubray
Perfectionnement en Pédiatrie (2024) Vol. 7, Iss. 1, pp. 75-83
Closed Access | Times Cited: 1
Jean‐Marie Saudubray
Perfectionnement en Pédiatrie (2024) Vol. 7, Iss. 1, pp. 75-83
Closed Access | Times Cited: 1
Cellular mechanisms of acute rhabdomyolysis in inherited metabolic diseases
Hortense de Calbiac, Apolline Imbard, Pascale de Lonlay
Journal of Inherited Metabolic Disease (2024) Vol. 48, Iss. 1
Closed Access | Times Cited: 1
Hortense de Calbiac, Apolline Imbard, Pascale de Lonlay
Journal of Inherited Metabolic Disease (2024) Vol. 48, Iss. 1
Closed Access | Times Cited: 1
Evaluation of Body Composition, Physical Activity, and Food Intake in Patients with Inborn Errors of Intermediary Metabolism
María-José de Castro, Paula Sánchez‐Pintos, Nisreem Abdelaziz-Salem, et al.
Nutrients (2021) Vol. 13, Iss. 6, pp. 2111-2111
Open Access | Times Cited: 10
María-José de Castro, Paula Sánchez‐Pintos, Nisreem Abdelaziz-Salem, et al.
Nutrients (2021) Vol. 13, Iss. 6, pp. 2111-2111
Open Access | Times Cited: 10
Clinical Approach to Inborn Errors of Metabolism in Paediatrics
Jean‐Marie Saudubray, Ángeles García‐Cazorla
Springer eBooks (2022), pp. 3-123
Closed Access | Times Cited: 7
Jean‐Marie Saudubray, Ángeles García‐Cazorla
Springer eBooks (2022), pp. 3-123
Closed Access | Times Cited: 7
