Cited In for PMID: 35847427

Your saved search

Your RSS Feed

Year	Number of Results
2022	1
2023	1
2025	1
2026	0

Results by year

Page 1

A case of severe acidosis in a 12-month-old: Succinyl-CoA:3-ketoacid-CoA transferase deficiency with OXCT1 gene mutations.

Dhammi N, Essakow J, Gallagher R, Gaw C. Dhammi N, et al. SAGE Open Med Case Rep. 2022 Jul 12;10:2050313X221111274. doi: 10.1177/2050313X221111274. eCollection 2022. SAGE Open Med Case Rep. 2022. PMID: 35847427 Free PMC article.

Pancrelipase as Adjunctive Therapy in Severe SCOT Deficiency: A Case of a Novel OXCT1 Gene Deletion.

Hamdeh MA, Jaber L, Abdullah J, Manhal A, Qouqas MM, Aldwaik M, Rmeilah SA, Sultan M, Shweiki S, Damseh N. Hamdeh MA, et al. JIMD Rep. 2025 May 22;66(3):e70024. doi: 10.1002/jmd2.70024. eCollection 2025 May. JIMD Rep. 2025. PMID: 40406160 Free PMC article.

SCOT Deficiency - A Fatal Metabolic Disorder Treated with Peritoneal Dialysis.

Chandran P, Kc S, Mp J, Am S. Chandran P, et al. Indian J Pediatr. 2023 May;90(5):528. doi: 10.1007/s12098-023-04546-4. Epub 2023 Mar 23. Indian J Pediatr. 2023. PMID: 36949368 No abstract available.

Page of 1

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3 results

Results by year

Filters

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Cited In for PMID: 35847427

3 results

Results by year