OpenAlex Citation Counts

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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:

The Respiratory Phenotype of Pompe Disease Mouse Models
Anna Fusco, Angela L. McCall, Justin Dhindsa, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 6, pp. 2256-2256
Open Access | Times Cited: 14

Showing 14 citing articles:

An emerging phenotype of central nervous system involvement in Pompe disease: from bench to bedside and beyond
Aditi Korlimarla, Jeong‐A Lim, Priya S. Kishnani, et al.
Annals of Translational Medicine (2019) Vol. 7, Iss. 13, pp. 289-289
Open Access | Times Cited: 56

Current treatment options and novel nanotechnology-driven enzyme replacement strategies for lysosomal storage disorders
Ambra Del Grosso, Gabriele Parlanti, Roberta Mezzena, et al.
Advanced Drug Delivery Reviews (2022) Vol. 188, pp. 114464-114464
Closed Access | Times Cited: 28

Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7
Anna Fusco, Logan A. Pucci, Paweł M. Świtoński, et al.
Disease Models & Mechanisms (2021) Vol. 14, Iss. 7
Open Access | Times Cited: 14

What’s new and what’s next for gene therapy in Pompe disease?
Angela L. Roger, Ronit Sethi, Meredith L. Huston, et al.
Expert Opinion on Biological Therapy (2022) Vol. 22, Iss. 9, pp. 1117-1135
Open Access | Times Cited: 9

Diaphragm weakness in late-onset Pompe disease: A complex interplay between lower motor neuron and muscle fibre degeneration
Miguel Oliveira Santos, Sara Domingues, Catarina Falcão de Campos, et al.
Journal of the Neurological Sciences (2024) Vol. 460, pp. 123021-123021
Closed Access | Times Cited: 1

GAA deficiency disrupts distal airway cells in Pompe disease
Léa El Haddad, Elias Lai, Preetish Kadur Lakshminarasimha Murthy, et al.
AJP Lung Cellular and Molecular Physiology (2023) Vol. 325, Iss. 3, pp. L288-L298
Open Access | Times Cited: 3

Infantile Pompe disease with intrauterine onset: a case report and literature review
Hongmin Xi, Xianghong Li, Lili Ma, et al.
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2022) Vol. 48, Iss. 1
Open Access | Times Cited: 2

Induced pluripotent stem cell for modeling Pompe disease
Wenjun Huang, Yanmin Zhang, Rui Zhou
Frontiers in Cardiovascular Medicine (2022) Vol. 9
Open Access | Times Cited: 2

The Respiratory Phenotype of Pompe Disease Rodent Models
Anna Fusco, Angela L. McCall, Justin Dhindsa, et al.
(2020)
Open Access | Times Cited: 2

Airway abnormalities and pulmonary complications in long‐term treated late‐onset Pompe disease: Diagnostic and interventional by flexible bronchoscopy
Ting‐Hao Wang, Wen‐Jue Soong, Dau‐Ming Niu, et al.
Pediatric Pulmonology (2021) Vol. 57, Iss. 1, pp. 185-192
Closed Access | Times Cited: 1

High-specific activity variants of recombinant human α-glucosidase for the treatment of Pompe disease
Anirudha Lakshminarasimhan
Medical Hypotheses (2023) Vol. 173, pp. 111044-111044
Closed Access

[Research progress of nervous system damage in Pompe disease].
Wenchao Zhang, Ying-ying MAO, Qian Chen
PubMed (2023) Vol. 25, Iss. 4, pp. 420-424
Closed Access

Pathophysiology of Lysosomes in a Nutshell
Ciro Isidoro
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 13, pp. 10688-10688
Open Access

A case of infantile Pompe disease with intrauterine onset and literature review
Hongmin Xi, Xianghong Li, Lili Ma, et al.
Research Square (Research Square) (2022)
Open Access

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