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For:	Baothman A, Almalki H, Abumelha K, Alshegifi A, Baashar A. Type 5 Familial Hemophagocytic Lymphohistiocytosis in a Seven-year-old Girl Post Second Bone Marrow Transplantation with Failure to Thrive: STXBP2 Novel Mutation. Cureus 2019;11:e6246. [PMID: 31807395 DOI: 10.7759/cureus.6246] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]

For:

Baothman A, Almalki H, Abumelha K, Alshegifi A, Baashar A. Type 5 Familial Hemophagocytic Lymphohistiocytosis in a Seven-year-old Girl Post Second Bone Marrow Transplantation with Failure to Thrive: STXBP2 Novel Mutation. Cureus 2019;11:e6246. [PMID: 31807395 DOI: 10.7759/cureus.6246] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]

Number	Citing Articles
1	Ahmari AA, Alsmadi O, Sheereen A, Elamin T, Jabr A, El-Baik L, Alhissi S, Saud BA, Al-Awwami M, Fawaz IA, Ayas M, Siddiqui K, Hawwari A. Genetic and clinical characteristics of pediatric patients with familial hemophagocytic lymphohistiocytosis. Blood Res 2021;56:86-101. [PMID: 34083498 DOI: 10.5045/br.2021.2020308] [Reference Citation Analysis]
2	Thadchanamoorthy V, Jayatunga MTR, Dayasiri K, Jasinge E, Jinnah MLM, Pereira C, Skrahina V, Thirukumar M. Exome sequencing detected an extremely rare case of foetal onset familial haemophagocytic lymphohistiocytosis type 5 presenting with hydrops foetalis. BMC Med Genomics 2021;14:50. [PMID: 33593331 DOI: 10.1186/s12920-021-00897-z] [Reference Citation Analysis]