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Development and Validation of Artificial Intelligence Models for Prognosis Prediction of Juvenile Myoclonic Epilepsy with Clinical and Radiological Features.

• Authors : Kim, Kyung Min¹ (AUTHOR); Choi, Bo Kyu^1,2 (AUTHOR); Ha, Woo-Seok¹ (AUTHOR)

• Source: Journal of Clinical Medicine. Sep2024, Vol. 13 Issue 17, p5080. 9p.

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Myoclonus improvement after seizures in progressive myoclonic epilepsy type 7: a case report.

• Authors : G S B Lima PL; Faculty of Medicine, Federal University of Ceara, Fortaleza, Ceara, Brazil.; Nobrega PR

Subjects: Myoclonic Epilepsies, Progressive*/Myoclonic Epilepsies, Progressive*/Myoclonic Epilepsies, Progressive*/complications ; Myoclonic Epilepsies, Progressive*/Myoclonic Epilepsies, Progressive*/Myoclonic Epilepsies, Progressive*/diagnosis ; Seizures*/Seizures*/Seizures*/diagnosis

• Source: BMC neurology [BMC Neurol] 2024 May 23; Vol. 24 (1), pp. 169. Date of Electronic Publication: 2024 May 23.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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A systematic review and meta-analysis of factors related to first line drugs refractoriness in patients with juvenile myoclonic epilepsy (JME).

• Authors : Fayad C; Department of Biology, Faculty of Arts and Sciences, Holy Spirit University of Kaslik-Jounieh, Lebanon.; Saad K

Subjects: Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/drug therapy ; Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/epidemiology ; Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/genetics

• Source: PloS one [PLoS One] 2024 Apr 09; Vol. 19 (4), pp. e0300930. Date of Electronic Publication: 2024 Apr 09 (Print Publication: 2024).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Association of variants in the ABCB1, CYP2C19 and CYP2C9 genes for Juvenile Myoclonic Epilepsy.

• Authors : Jara-Prado A; Genetics Department, National Institute of Neurology and Neurosurgery, Mexico City, Mexico.; Guerrero-Camacho JL

Subjects: Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/genetics ; Epilepsy, Generalized*; Male

• Source: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2024 Apr; Vol. 45 (4), pp. 1635-1643. Publisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Sarcopenia and anti-seizure medication response in juvenile myoclonic epilepsy.

• Authors : Kim J; Department of Family Medicine, Busan Paik Hospital, Inje University College of Medicine, Busan, Republic of Korea.; Lee HJ

Subjects: Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/complications ; Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/diagnostic imaging ; Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/Myoclonic Epilepsy, Juvenile*/drug therapy

• Source: Brain and behavior [Brain Behav] 2024 Mar; Vol. 14 (3), pp. e3464.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101570837 Publication Model: Print Cited Medium: Internet ISSN:

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A case of a 6-year-old girl with a rare compound heterozygous mutation of KCTD7 presenting with progressive myoclonic epilepsy.

• Authors : Badv, Reza Shervin¹ (AUTHOR); Shariatmadari, Fakhreddin^1,2 (AUTHOR); Bayat, Shiva³ (AUTHOR)

Subjects: *MYOCLONUS; *POTASSIUM channels; *ETIOLOGY of diseases

• Source: Egyptian Journal of Medical Human Genetics. 11/4/2024, Vol. 25 Issue 1, p1-4. 4p.

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Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findings

• Authors : Lassana Cissé; Salia Bamba; Seybou H. Diallo

Subjects: progressive myoclonic epilepsy; genetic; novel variants

• Source: Frontiers in Neurology, Vol 15 (2024)

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Progressive myoclonic ataxia as an initial symptom of typical type I sialidosis with NEU1 mutation.

• Authors : Lin, Jingjing¹ (AUTHOR); Li, Yun‐Lu¹ (AUTHOR); Chen, Bo‐Li¹ (AUTHOR)

• Source: Annals of Clinical & Translational Neurology. Nov2024, Vol. 11 Issue 11, p2998-3009. 12p.

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Seizures and electrophysiological features in familial cortical myoclonic tremor with epilepsy 1.

• Authors : Ding Y; Department of Neurology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.; Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.

Subjects: Epilepsy* ; Epilepsies, Myoclonic*/Epilepsies, Myoclonic*/Epilepsies, Myoclonic*/genetics; Humans Epilepsy, Myoclonic, Benign Adult Familial, Type 1

• Source: Annals of clinical and translational neurology [Ann Clin Transl Neurol] 2024 Feb; Vol. 11 (2), pp. 414-423. Date of Electronic Publication: 2023 Dec 07.Publisher: Wiley Periodicals, Inc on behalf of American Neurological Association Country of Publication: United States NLM ID: 101623278 Publication Model:

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The Roles of Cystatin B in the Brain and Pathophysiological Mechanisms of Progressive Myoclonic Epilepsy Type 1.

• Authors : Singh S; A.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Neulaniementie 2, 70211 Kuopio, Finland.; Hämäläinen RH

Subjects: Cystatin B*/Cystatin B*/Cystatin B*/genetics ; Myoclonic Epilepsies, Progressive*/Myoclonic Epilepsies, Progressive*/Myoclonic Epilepsies, Progressive*/genetics ; Unverricht-Lundborg Syndrome*

• Source: Cells [Cells] 2024 Jan 16; Vol. 13 (2). Date of Electronic Publication: 2024 Jan 16.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101600052 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4409

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