صرع رمعي عضلي شبابي (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "صرع رمعي عضلي شبابي" in Arabic language version.

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18nih.gov

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12doi.org

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1medscape.com

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1books.google.com

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books.google.com

Janz، D.؛ Christian، W. (1994). "Impulsive petit mal". في Malafosse، Alain (المحرر). Idiopathic Generalized Epilepsies: Clinical, Experimental and Genetic Aspects. ص. 229–51. ISBN:978-0-86196-436-9.

doi.org

Scheffer, IE؛ Berkovic, S؛ Capovilla, G.؛ Connolly, MB؛ French, J؛ Guilhoto, L.؛ Hirsch, E.؛ Jain, S.؛ Mathern, GN؛ Moshe', SL؛ Norolli, DR؛ Perucca, E؛ Tomson, T؛ Wiebe, S؛ Zhang, YH؛ Zuberi, SM (2017). "ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology". Epilepsia. ج. 58 ع. 4: 512–521. DOI:10.1111/epi.13709. PMC:5386840. PMID:28276062.
Panayiotopoulos, CP؛ Obeid, T؛ Tahan, AR (1994). "Juvenile myoclonic epilepsy: a 5-year prospective study". Epilepsia. ج. 35 ع. 2: 285–296. DOI:10.1111/j.1528-1157.1994.tb02432.x. PMID:8156946.
Camfield, CS؛ Striano, P؛ Camfield, PR (2013). "Epidemiology of juvenile myoclonic epilepsy". Epilepsy Behav. 28 Suppl. 1: S15–17. DOI:10.1016/j.yebeh.2012.06.024. PMID:23756473.
Syvertsen, M؛ Hellum, MK؛ Hansen, G؛ Edland, A؛ Nakken, KO؛ Selmer, KK؛ Koht, J. (2017). "Prevalence of juvenile myoclonic epilepsy in people <30 years of age-A population-based study in Norway". Epilepsia. ج. 58 ع. 1: 105–112. DOI:10.1111/epi.13613. PMID:27861775.
Delgado-Escueta, AV؛ Koeleman, BP؛ Bailey, J؛ Medina, MT؛ Duron, RM (2013). "The quest for juvenile myoclonic epilepsy genes". Epilepsy Behav. 28 Suppl 1: S52-7. DOI:10.1016/j.yebeh.2012.06.033. PMID:23756480.
Kasteleijn-Nolst Trenite, DG؛ de Weerd, A؛ Beniczky, S (2013). "Chronodependency and provocative factors in juvenile myoclonic epilepsy". Epilepsy Behav. 28 Suppl 1: S25-9. DOI:10.1016/j.yebeh.2012.11.045. PMID:23756476.
Escayg, A؛ De Waard, M؛ Lee, DD؛ Bichet, D؛ Wolf, P؛ Mayer, T؛ Johnston, J؛ Baloh, R؛ Sander, T؛ Meisler, MH (2000). "Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia". Am J Hum Genet. ج. 66 ع. 5: 1531–1539. DOI:10.1086/302909. PMC:1378014. PMID:10762541.
Etemad, S؛ Campiglio, M؛ Obermair, GJ؛ Flucher, BE (2014). "The juvenile myoclonic epilepsy mutant of the calcium channel beta(4) subunit displays normal nuclear targeting in nerve and muscle cells". Channels. ج. 8 ع. 4: 334–343. DOI:10.4161/chan.29322. PMC:4203735. PMID:24875574.
Delgado-Escueta, AV (2007). "Advances in genetics of juvenile myoclonic epilepsies". Epilepsy Curr. ج. 7 ع. 3: 61–67. DOI:10.1111/j.1535-7511.2007.00171.x. PMC:1874323. PMID:17520076.
Cossette P، Liu L، Brisebois K، Dong H، Lortie A، Vanasse M، Saint-Hilaire J، Carmant L، Verner A، Lu W، Wang Y، Rouleau G (2002). "Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy". Nat Genet. ج. 31 ع. 2: 184–189. DOI:10.1038/ng885. PMID:11992121.
Grünewald، R. A.؛ Chroni، E.؛ Panayiotopoulos، C. P. (يونيو 1992). "Delayed diagnosis of juvenile myoclonic epilepsy". J. Neurol. Neurosurg. Psychiatry. ج. 55 ع. 6: 497–9. DOI:10.1136/jnnp.55.6.497. PMC:1014908. PMID:1619419.
Kim, JH (2017). "Grey and White Matter Alterations in Juvenile Myoclonic Epilepsy: A Comprehensive Review". J. Epilepsy Res. ج. 7 ع. 2: 77–88. DOI:10.14581/jer.17013. PMC:5767493. PMID:29344465.

medscape.com

emedicine.medscape.com

Juvenile Myoclonic Epilepsy في موقع إي ميديسين

nih.gov

pubmed.ncbi.nlm.nih.gov

Scheffer, IE؛ Berkovic, S؛ Capovilla, G.؛ Connolly, MB؛ French, J؛ Guilhoto, L.؛ Hirsch, E.؛ Jain, S.؛ Mathern, GN؛ Moshe', SL؛ Norolli, DR؛ Perucca, E؛ Tomson, T؛ Wiebe, S؛ Zhang, YH؛ Zuberi, SM (2017). "ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology". Epilepsia. ج. 58 ع. 4: 512–521. DOI:10.1111/epi.13709. PMC:5386840. PMID:28276062.
Panayiotopoulos, CP؛ Obeid, T؛ Tahan, AR (1994). "Juvenile myoclonic epilepsy: a 5-year prospective study". Epilepsia. ج. 35 ع. 2: 285–296. DOI:10.1111/j.1528-1157.1994.tb02432.x. PMID:8156946.
Camfield, CS؛ Striano, P؛ Camfield, PR (2013). "Epidemiology of juvenile myoclonic epilepsy". Epilepsy Behav. 28 Suppl. 1: S15–17. DOI:10.1016/j.yebeh.2012.06.024. PMID:23756473.
Syvertsen, M؛ Hellum, MK؛ Hansen, G؛ Edland, A؛ Nakken, KO؛ Selmer, KK؛ Koht, J. (2017). "Prevalence of juvenile myoclonic epilepsy in people <30 years of age-A population-based study in Norway". Epilepsia. ج. 58 ع. 1: 105–112. DOI:10.1111/epi.13613. PMID:27861775.
Delgado-Escueta, AV؛ Koeleman, BP؛ Bailey, J؛ Medina, MT؛ Duron, RM (2013). "The quest for juvenile myoclonic epilepsy genes". Epilepsy Behav. 28 Suppl 1: S52-7. DOI:10.1016/j.yebeh.2012.06.033. PMID:23756480.
Kasteleijn-Nolst Trenite, DG؛ de Weerd, A؛ Beniczky, S (2013). "Chronodependency and provocative factors in juvenile myoclonic epilepsy". Epilepsy Behav. 28 Suppl 1: S25-9. DOI:10.1016/j.yebeh.2012.11.045. PMID:23756476.
Escayg, A؛ De Waard, M؛ Lee, DD؛ Bichet, D؛ Wolf, P؛ Mayer, T؛ Johnston, J؛ Baloh, R؛ Sander, T؛ Meisler, MH (2000). "Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia". Am J Hum Genet. ج. 66 ع. 5: 1531–1539. DOI:10.1086/302909. PMC:1378014. PMID:10762541.
Etemad, S؛ Campiglio, M؛ Obermair, GJ؛ Flucher, BE (2014). "The juvenile myoclonic epilepsy mutant of the calcium channel beta(4) subunit displays normal nuclear targeting in nerve and muscle cells". Channels. ج. 8 ع. 4: 334–343. DOI:10.4161/chan.29322. PMC:4203735. PMID:24875574.
Delgado-Escueta, AV (2007). "Advances in genetics of juvenile myoclonic epilepsies". Epilepsy Curr. ج. 7 ع. 3: 61–67. DOI:10.1111/j.1535-7511.2007.00171.x. PMC:1874323. PMID:17520076.
Cossette P، Liu L، Brisebois K، Dong H، Lortie A، Vanasse M، Saint-Hilaire J، Carmant L، Verner A، Lu W، Wang Y، Rouleau G (2002). "Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy". Nat Genet. ج. 31 ع. 2: 184–189. DOI:10.1038/ng885. PMID:11992121.
Grünewald، R. A.؛ Chroni، E.؛ Panayiotopoulos، C. P. (يونيو 1992). "Delayed diagnosis of juvenile myoclonic epilepsy". J. Neurol. Neurosurg. Psychiatry. ج. 55 ع. 6: 497–9. DOI:10.1136/jnnp.55.6.497. PMC:1014908. PMID:1619419.
Kim, JH (2017). "Grey and White Matter Alterations in Juvenile Myoclonic Epilepsy: A Comprehensive Review". J. Epilepsy Res. ج. 7 ع. 2: 77–88. DOI:10.14581/jer.17013. PMC:5767493. PMID:29344465.

ncbi.nlm.nih.gov

Scheffer, IE؛ Berkovic, S؛ Capovilla, G.؛ Connolly, MB؛ French, J؛ Guilhoto, L.؛ Hirsch, E.؛ Jain, S.؛ Mathern, GN؛ Moshe', SL؛ Norolli, DR؛ Perucca, E؛ Tomson, T؛ Wiebe, S؛ Zhang, YH؛ Zuberi, SM (2017). "ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology". Epilepsia. ج. 58 ع. 4: 512–521. DOI:10.1111/epi.13709. PMC:5386840. PMID:28276062.
Escayg, A؛ De Waard, M؛ Lee, DD؛ Bichet, D؛ Wolf, P؛ Mayer, T؛ Johnston, J؛ Baloh, R؛ Sander, T؛ Meisler, MH (2000). "Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia". Am J Hum Genet. ج. 66 ع. 5: 1531–1539. DOI:10.1086/302909. PMC:1378014. PMID:10762541.
Etemad, S؛ Campiglio, M؛ Obermair, GJ؛ Flucher, BE (2014). "The juvenile myoclonic epilepsy mutant of the calcium channel beta(4) subunit displays normal nuclear targeting in nerve and muscle cells". Channels. ج. 8 ع. 4: 334–343. DOI:10.4161/chan.29322. PMC:4203735. PMID:24875574.
Delgado-Escueta, AV (2007). "Advances in genetics of juvenile myoclonic epilepsies". Epilepsy Curr. ج. 7 ع. 3: 61–67. DOI:10.1111/j.1535-7511.2007.00171.x. PMC:1874323. PMID:17520076.
Grünewald، R. A.؛ Chroni، E.؛ Panayiotopoulos، C. P. (يونيو 1992). "Delayed diagnosis of juvenile myoclonic epilepsy". J. Neurol. Neurosurg. Psychiatry. ج. 55 ع. 6: 497–9. DOI:10.1136/jnnp.55.6.497. PMC:1014908. PMID:1619419.
Kim, JH (2017). "Grey and White Matter Alterations in Juvenile Myoclonic Epilepsy: A Comprehensive Review". J. Epilepsy Res. ج. 7 ع. 2: 77–88. DOI:10.14581/jer.17013. PMC:5767493. PMID:29344465.