Works matching IS 17088569 AND DT 2023 AND VI 19 AND IP 7
Results: 10
Delayed-onset adenosine deaminase deficiency with a novel synonymous mutation and a case series from China.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 7, p. 687, doi. 10.1007/s12519-023-00729-3
- By:
- Publication type:
- Article
Response to "Incidence and severity of pediatric appendicitis during the COVID‑19 pandemic".
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 7, p. 713, doi. 10.1007/s12519-023-00713-x
- By:
- Publication type:
- Article
Incidence and severity of pediatric appendicitis during the COVID‑19 pandemic.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 7, p. 710, doi. 10.1007/s12519-023-00712-y
- By:
- Publication type:
- Article
Comprehensive characterization of the genetic landscape of familial Hirschsprung's disease.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 7, p. 644, doi. 10.1007/s12519-023-00686-x
- By:
- Publication type:
- Article
Inherited Fanconi syndrome.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 7, p. 619, doi. 10.1007/s12519-023-00685-y
- By:
- Publication type:
- Article
Clinical spectrum and currently available treatment of type I interferonopathy Aicardi–Goutières syndrome.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 7, p. 635, doi. 10.1007/s12519-022-00679-2
- By:
- Publication type:
- Article
Poly-hydroxylated bile acids and their prognostic roles in Alagille syndrome.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 7, p. 652, doi. 10.1007/s12519-022-00676-5
- By:
- Publication type:
- Article
Australian children living with rare diseases: health service use and barriers to accessing care.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 7, p. 701, doi. 10.1007/s12519-022-00675-6
- By:
- Publication type:
- Article
Unique mutation spectrum of progressive pseudorheumatoid dysplasia in the Chinese population: a retrospective genotype–phenotype analysis of 105 patients.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 7, p. 674, doi. 10.1007/s12519-022-00674-7
- By:
- Publication type:
- Article
A multicenter prospective study of next-generation sequencing-based newborn screening for monogenic genetic diseases in China.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 7, p. 663, doi. 10.1007/s12519-022-00670-x
- By:
- Publication type:
- Article