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Cited by in F6Publishing
For: Di Bella D, Magri S, Benzoni C, Farina L, Maccagnano C, Sarto E, Moscatelli M, Baratta S, Ciano C, Piacentini SHMJ, Draghi L, Mauro E, Pareyson D, Gellera C, Taroni F, Salsano E. Hypomyelinating leukodystrophies in adults: Clinical and genetic features. Eur J Neurol 2021;28:934-44. [PMID: 33190326 DOI: 10.1111/ene.14646] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Hashiguchi M, Monden Y, Nozaki Y, Watanabe K, Nakashima M, Saitsu H, Yamagata T, Osaka H. A TUBB4A Met363Thr variant in pediatric hypomyelination without atrophy of the basal ganglia. Hum Genome Var 2022;9:19. [PMID: 35661708 DOI: 10.1038/s41439-022-00198-6] [Reference Citation Analysis]
2 Verdura E, Rodríguez-Palmero A, Vélez-Santamaria V, Planas-Serra L, de la Calle I, Raspall-Chaure M, Roubertie A, Benkirane M, Saettini F, Pavinato L, Mandrile G, O'Leary M, O'Heir E, Barredo E, Chacón A, Michaud V, Goizet C, Ruiz M, Schlüter A, Rouvet I, Sala-Coromina J, Fossati C, Iascone M, Canonico F, Marcé-Grau A, de Souza P, Adams DR, Casasnovas C, Rehm HL, Mefford HC, González Gutierrez-Solana L, Brusco A, Koenig M, Macaya A, Pujol A. Biallelic PI4KA variants cause a novel neurodevelopmental syndrome with hypomyelinating leukodystrophy. Brain 2021;144:2659-69. [PMID: 34415322 DOI: 10.1093/brain/awab124] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
3 Quitmann CM, Rust S, Reunert J, Biskup S, Fiedler B, Marquardt T. Tubulin Folding Cofactor D Deficiency: Missing the Diagnosis With Whole Exome Sequencing. Child Neurol Open 2021;8:2329048X211034969. [PMID: 34423067 DOI: 10.1177/2329048X211034969] [Reference Citation Analysis]
4 Mochel F. Hypomyelinating leukodystrophies in adults. Eur J Neurol 2021;28:733-4. [PMID: 33400842 DOI: 10.1111/ene.14694] [Reference Citation Analysis]