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:
Clinical Therapeutic Management of Human Mitochondrial Disorders
Josef Finsterer
Pediatric Neurology (2020) Vol. 113, pp. 66-74
Closed Access | Times Cited: 8
Josef Finsterer
Pediatric Neurology (2020) Vol. 113, pp. 66-74
Closed Access | Times Cited: 8
Showing 8 citing articles:
Mitochondrial regulatory mechanisms in spinal cord injury: A narrative review
Chengjiang Liu, Yidong Liu, Boyuan Ma, et al.
Medicine (2022) Vol. 101, Iss. 46, pp. e31930-e31930
Open Access | Times Cited: 13
Chengjiang Liu, Yidong Liu, Boyuan Ma, et al.
Medicine (2022) Vol. 101, Iss. 46, pp. e31930-e31930
Open Access | Times Cited: 13
Practice of Multidisciplinary Collaborative Chain Management Model in Constructing Nursing Path for Acute Trauma Treatment
Shuangqiong Xiang, Weiping Tang, Xiaoyuan Shang, et al.
Emergency Medicine International (2022) Vol. 2022, pp. 1-5
Open Access | Times Cited: 5
Shuangqiong Xiang, Weiping Tang, Xiaoyuan Shang, et al.
Emergency Medicine International (2022) Vol. 2022, pp. 1-5
Open Access | Times Cited: 5
Respiratory chain defects require prospective work‐up for clinical and subclinical multisystem involvement
Josef Finsterer
Pediatric Dermatology (2023) Vol. 40, Iss. 6, pp. 1168-1169
Closed Access | Times Cited: 1
Josef Finsterer
Pediatric Dermatology (2023) Vol. 40, Iss. 6, pp. 1168-1169
Closed Access | Times Cited: 1
Precision mitochondrial medicine: Uncovering pathways across diverse diseases
Lourdes Sainero‐Alcolado, Elisa Garde-Lapido, Judit Liaño-Pons, et al.
Elsevier eBooks (2024), pp. 115-169
Closed Access
Lourdes Sainero‐Alcolado, Elisa Garde-Lapido, Judit Liaño-Pons, et al.
Elsevier eBooks (2024), pp. 115-169
Closed Access
Clinical exome sequencing reveals a mutation in PDHA1 in Leigh syndrome: A case of a Chinese boy with lethal neuropathy
Ke Gong, Lixin Xie, Zhong‐shi Wu, et al.
Molecular Genetics & Genomic Medicine (2021) Vol. 9, Iss. 4
Open Access | Times Cited: 2
Ke Gong, Lixin Xie, Zhong‐shi Wu, et al.
Molecular Genetics & Genomic Medicine (2021) Vol. 9, Iss. 4
Open Access | Times Cited: 2
Types of neuromuscular disease
John F. Brandsema, Susan Matesanz
Elsevier eBooks (2023), pp. 3-22
Closed Access
John F. Brandsema, Susan Matesanz
Elsevier eBooks (2023), pp. 3-22
Closed Access
Personalized medicine – parenteral ketogenic diet in pyruvate dehydrogenase deficiency in the ICU; what do we need to know about it?
Mileva Frankić, Sanda Stojanović Stipić, Toni Kljaković Gašpić, et al.
Liječnički vjesnik (2022) Vol. 144, Iss. Supp 3
Open Access
Mileva Frankić, Sanda Stojanović Stipić, Toni Kljaković Gašpić, et al.
Liječnički vjesnik (2022) Vol. 144, Iss. Supp 3
Open Access
m.3243A>G Maculopathy
Josef Finsterer
Klinische Monatsblätter für Augenheilkunde (2021) Vol. 238, Iss. 07, pp. 827-827
Closed Access
Josef Finsterer
Klinische Monatsblätter für Augenheilkunde (2021) Vol. 238, Iss. 07, pp. 827-827
Closed Access
