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For: Stregapede F, Travaglini L, Rebelo AP, Cintra VP, Bellacchio E, Bosco L, Alfieri P, Pro S, Zuchner S, Bertini E, Nicita F. Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation. Clin Genet 2019;97:521-6. [DOI: 10.1111/cge.13668] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
Number Citing Articles
1 Konrad M, Schlingmann KP. Inherited Disorders of Renal Magnesium Handling. Pediatric Nephrology 2022. [DOI: 10.1007/978-3-030-52719-8_109] [Reference Citation Analysis]
2 Jiao S, Johnson K, Moreno C, Yano S, Holmgren M. Comparative description of the mRNA expression profile of Na+ /K+ -ATPase isoforms in adult mouse nervous system. J Comp Neurol 2021. [PMID: 34415061 DOI: 10.1002/cne.25234] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
3 Elayadeth-Meethal M, Thazhathu Veettil A, Asaf M, Pramod S, Maloney SK, Martin GB, Rivero MJ, Sejian V, Naseef PP, Kuruniyan MS, Lee MRF. Comparative Expression Profiling and Sequence Characterization of ATP1A1 Gene Associated with Heat Tolerance in Tropically Adapted Cattle. Animals (Basel) 2021;11:2368. [PMID: 34438824 DOI: 10.3390/ani11082368] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
4 Argente-Escrig H, Frasquet M, Vázquez-Costa JF, Millet-Sancho E, Pitarch I, Tomás-Vila M, Espinós C, Lupo V, Sevilla T. Pediatric inherited peripheral neuropathy: a prospective study at a Spanish referral center. Ann Clin Transl Neurol 2021;8:1809-16. [PMID: 34323022 DOI: 10.1002/acn3.51432] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
5 Biondo ED, Spontarelli K, Ababioh G, Méndez L, Artigas P. Diseases caused by mutations in the Na+/K+ pump α1 gene ATP1A1. Am J Physiol Cell Physiol 2021;321:C394-408. [PMID: 34232746 DOI: 10.1152/ajpcell.00059.2021] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
6 Lin Z, Li J, Ji T, Wu Y, Gao K, Jiang Y. ATP1A1 de novo Mutation-Related Disorders: Clinical and Genetic Features. Front Pediatr 2021;9:657256. [PMID: 33968856 DOI: 10.3389/fped.2021.657256] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
7 Konrad M, Schlingmann KP. Inherited Disorders of Renal Magnesium Handling. Pediatric Nephrology 2021. [DOI: 10.1007/978-3-642-27843-3_109-1] [Reference Citation Analysis]