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For: Bohlega SA, Abou-al-shaar H, Aldakheel A, Alajlan H, Bohlega BS, Meyer BF, Monies D, Cupler EJ, Al-saif AM. Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders. Parkinsonism & Related Disorders 2019;64:145-9. [DOI: 10.1016/j.parkreldis.2019.02.039] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 3.7] [Reference Citation Analysis]
Number Citing Articles
1 Piard J, Béreau M, XiangWei W, Wirth T, Amsallem D, Buisson L, Richard P, Liu N, Xu Y, Myers SJ, Traynelis SF, Chelly J, Anheim M, Raynaud M, Maldergem LV, Yuan H. The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus. Mov Disord 2020;35:1224-32. [PMID: 32369665 DOI: 10.1002/mds.28058] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
2 Gannamani R, van der Veen S, van Egmond M, de Koning TJ, Tijssen MAJ. Challenges in Clinicogenetic Correlations: One Phenotype - Many Genes. Mov Disord Clin Pract 2021;8:311-21. [PMID: 33816658 DOI: 10.1002/mdc3.13163] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
3 Okamoto N, Miya F, Kitai Y, Tsunoda T, Kato M, Saitoh S, Kanemura Y, Kosaki K. Homozygous ADCY5 mutation causes early-onset movement disorder with severe intellectual disability. Neurol Sci 2021;42:2975-8. [PMID: 33704598 DOI: 10.1007/s10072-021-05152-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Kaiyrzhanov R, Zaki MS, Maroofian R, Dominik N, Rad A, Vona B, Houlden H. A Novel Homozygous ADCY5 Variant is Associated with a Neurodevelopmental Disorder and Movement Abnormalities. Mov Disord Clin Pract 2021;8:1140-3. [PMID: 34631954 DOI: 10.1002/mdc3.13310] [Reference Citation Analysis]
5 Eisenberg HJ, Malinova V, Mielke D, Bähr M, Göricke MB, van Riesen C. ADCY5-Induced Dyskinetic Storm Rescued with Pallidal Deep Brain Stimulation in a 46-Year-Old Man. Mov Disord Clin Pract 2021;8:142-4. [PMID: 33426171 DOI: 10.1002/mdc3.13076] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
6 Harvey S, King MD, Gorman KM. Paroxysmal Movement Disorders. Front Neurol 2021;12:659064. [PMID: 34177764 DOI: 10.3389/fneur.2021.659064] [Reference Citation Analysis]
7 Garone G, Capuano A, Travaglini L, Graziola F, Stregapede F, Zanni G, Vigevano F, Bertini E, Nicita F. Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias. Int J Mol Sci 2020;21:E3603. [PMID: 32443735 DOI: 10.3390/ijms21103603] [Cited by in Crossref: 13] [Cited by in F6Publishing: 8] [Article Influence: 6.5] [Reference Citation Analysis]
8 Powis Z, Towne MC, Hagman KDF, Blanco K, Palmaer E, Castro A, Sajan SA, Radtke K, Feyma TJ, Juliette K, Tang S, Sidiropoulos C. Clinical diagnostic exome sequencing in dystonia: Genetic testing challenges for complex conditions. Clin Genet 2020;97:305-11. [PMID: 31628766 DOI: 10.1111/cge.13657] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.7] [Reference Citation Analysis]
9 Ferrini A, Steel D, Barwick K, Kurian MA. An Update on the Phenotype, Genotype and Neurobiology of ADCY5-Related Disease. Mov Disord 2021;36:1104-14. [PMID: 33934385 DOI: 10.1002/mds.28495] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Chen DH, Latimer CS, Spencer M, Karna P, Gonzalez-Cuyar LF, Davis MY, Keene CD, Bird TD, Raskind WH. Hyperphosphorylated Tau, Increased Adenylate Cyclase 5 (ADCY5) Immunoreactivity, but No Neuronal Loss in ADCY5-Dyskinesia. Mov Disord Clin Pract 2020;7:70-7. [PMID: 31970214 DOI: 10.1002/mdc3.12873] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
11 Vijiaratnam N, Bhatia KP, Lang AE, Raskind WH, Espay AJ. ADCY5-Related Dyskinesia: Improving Clinical Detection of an Evolving Disorder. Mov Disord Clin Pract 2019;6:512-20. [PMID: 31538084 DOI: 10.1002/mdc3.12816] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 4.7] [Reference Citation Analysis]