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Showing 1 to 12 of 81 entries
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[Problems of etiology and electroencephalography in childhood epilepsy].

Das Deutsche Gesundheitswesen

Degen R.
PMID: 5022770
Dtsch Gesundheitsw. 1972 Jan 13;27(2):71-6.

No abstract available.

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Degen R. Probleme der Atiologie und Elektroenzephalographie der kindlichen Epilepsie. [Problems of etiology and electroencephalography in childhood epilepsy]. Dtsch Gesundheitsw. 1972;27(2):71-6
Degen, R. (1972). Probleme der Atiologie und Elektroenzephalographie der kindlichen Epilepsie. [Problems of etiology and electroencephalography in childhood epilepsy]. Das Deutsche Gesundheitswesen, 27(2), 71-6.
Degen, R. "Probleme der Atiologie und Elektroenzephalographie der kindlichen Epilepsie." [Problems of etiology and electroencephalography in childhood epilepsy]. Das Deutsche Gesundheitswesen vol. 27,2 (1972): 71-6.
Degen R. Probleme der Atiologie und Elektroenzephalographie der kindlichen Epilepsie. [Problems of etiology and electroencephalography in childhood epilepsy]. Dtsch Gesundheitsw. 1972 Jan 13;27(2):71-6. German. PMID: 5022770.
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[Pathogenesis and etiology of epilepsy].

Hippokrates

Christian W.
PMID: 5730665
Hippokrates. 1968 Mar 15;39(5):157-64.

No abstract available.

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Christian W. Pathogenese und Atiologie der Epilepsien. [Pathogenesis and etiology of epilepsy]. Hippokrates. 1968;39(5):157-64
Christian, W. (1968). Pathogenese und Atiologie der Epilepsien. [Pathogenesis and etiology of epilepsy]. Hippokrates, 39(5), 157-64.
Christian, W. "Pathogenese und Atiologie der Epilepsien." [Pathogenesis and etiology of epilepsy]. Hippokrates vol. 39,5 (1968): 157-64.
Christian W. Pathogenese und Atiologie der Epilepsien. [Pathogenesis and etiology of epilepsy]. Hippokrates. 1968 Mar 15;39(5):157-64. German. PMID: 5730665.
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A unifying concept of idiopathic epilepsy.

Postgraduate medicine

Bray PF, Wiser WC.
PMID: 5791356
Postgrad Med. 1969 Jul;46(1):82-7. doi: 10.1080/00325481.1969.11697204.

No abstract available.

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Bray PF, Wiser WC. A unifying concept of idiopathic epilepsy. Postgrad Med. 1969;46(1):82-7doi: 10.1080/00325481.1969.11697204.
Bray, P. F., & Wiser, W. C. (1969). A unifying concept of idiopathic epilepsy. Postgraduate medicine, 46(1), 82-7. https://doi.org/10.1080/00325481.1969.11697204
Bray, P F, and Wiser, W C. "A unifying concept of idiopathic epilepsy." Postgraduate medicine vol. 46,1 (1969): 82-7. doi: https://doi.org/10.1080/00325481.1969.11697204
Bray PF, Wiser WC. A unifying concept of idiopathic epilepsy. Postgrad Med. 1969 Jul;46(1):82-7. doi: 10.1080/00325481.1969.11697204. PMID: 5791356.
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Risk Factors for Obstructive Sleep Apnea Syndrome in Genetic Epilepsy.

Indian journal of pediatrics

Gogou M, Pavlou E, Eboriadou M, Hatzistylianou M, Haidopoulou K.
PMID: 27345566
Indian J Pediatr. 2016 Nov;83(12):1497-1498. doi: 10.1007/s12098-016-2183-2. Epub 2016 Jun 27.

No abstract available.

Cite
Gogou M, Pavlou E, Eboriadou M, et al. Risk Factors for Obstructive Sleep Apnea Syndrome in Genetic Epilepsy. Indian J Pediatr. 2016;83(12):1497-1498doi: 10.1007/s12098-016-2183-2.
Gogou, M., Pavlou, E., Eboriadou, M., Hatzistylianou, M., & Haidopoulou, K. (2016). Risk Factors for Obstructive Sleep Apnea Syndrome in Genetic Epilepsy. Indian journal of pediatrics, 83(12), 1497-1498. https://doi.org/10.1007/s12098-016-2183-2
Gogou, Maria, et al. "Risk Factors for Obstructive Sleep Apnea Syndrome in Genetic Epilepsy." Indian journal of pediatrics vol. 83,12 (2016): 1497-1498. doi: https://doi.org/10.1007/s12098-016-2183-2
Gogou M, Pavlou E, Eboriadou M, Hatzistylianou M, Haidopoulou K. Risk Factors for Obstructive Sleep Apnea Syndrome in Genetic Epilepsy. Indian J Pediatr. 2016 Nov;83(12):1497-1498. doi: 10.1007/s12098-016-2183-2. Epub 2016 Jun 27. PMID: 27345566.
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Familial occurrence of focal temporal electroencephalographic abnormalities.

Neurology

RODIN EA, WHELAN JL.
PMID: 14438168
Neurology. 1960 Jun;10:542-5. doi: 10.1212/wnl.10.6.542.

No abstract available.

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RODIN EA, WHELAN JL. Familial occurrence of focal temporal electroencephalographic abnormalities. Neurology. 1960;10:542-5doi: 10.1212/wnl.10.6.542.
RODIN, E. A., & WHELAN, J. L. (1960). Familial occurrence of focal temporal electroencephalographic abnormalities. Neurology, 10542-5. https://doi.org/10.1212/wnl.10.6.542
RODIN, E A, and WHELAN, J L. "Familial occurrence of focal temporal electroencephalographic abnormalities." Neurology vol. 10 (1960): 542-5. doi: https://doi.org/10.1212/wnl.10.6.542
RODIN EA, WHELAN JL. Familial occurrence of focal temporal electroencephalographic abnormalities. Neurology. 1960 Jun;10:542-5. doi: 10.1212/wnl.10.6.542. PMID: 14438168.
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[Genetic anticipation in idiopathic epilepsies].

Revista de neurologia

Arcos-Burgos M, Palacio LG, Sánchez JL, Jiménez ME, Mora O, Zuluaga L, Uribe CS, López-Gartner G, Jiménez I.
PMID: 10599103
Rev Neurol. 1999 Oct 1-15;29(7):597-9.

INTRODUCTION: In extended and multigenerational pedigrees, the idiopathic epilepsy phenotype shows an extreme variability.OBJECTIVE: The range of idiopathic epilepsy onset age in multigenerational pedigrees was studied in order to determine if genetic anticipation play a role in the heredity...

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Arcos-Burgos M, Palacio LG, Sánchez JL, et al. Anticipación genética en epilepsia idiopática. [Genetic anticipation in idiopathic epilepsies]. Rev Neurol. 1999;29(7):597-9
Arcos-Burgos, M., Palacio, L. G., Sánchez, J. L., Jiménez, M. E., Mora, O., Zuluaga, L., Uribe, C. S., López-Gartner, G., & Jiménez, I. (1999). Anticipación genética en epilepsia idiopática. [Genetic anticipation in idiopathic epilepsies]. Revista de neurologia, 29(7), 597-9.
Arcos-Burgos, M, et al. "Anticipación genética en epilepsia idiopática." [Genetic anticipation in idiopathic epilepsies]. Revista de neurologia vol. 29,7 (1999): 597-9.
Arcos-Burgos M, Palacio LG, Sánchez JL, Jiménez ME, Mora O, Zuluaga L, Uribe CS, López-Gartner G, Jiménez I. Anticipación genética en epilepsia idiopática. [Genetic anticipation in idiopathic epilepsies]. Rev Neurol. 1999 Oct 1-15;29(7):597-9. Spanish. PMID: 10599103.
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Epilepsy in the families of epileptics.

The Journal of pediatrics

EISNER V, PAULI LL, LIVINGSTON S.
PMID: 13819783
J Pediatr. 1960 Mar;56:347-54. doi: 10.1016/s0022-3476(60)80186-2.

No abstract available.

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EISNER V, PAULI LL, LIVINGSTON S. Epilepsy in the families of epileptics. J Pediatr. 1960;56:347-54doi: 10.1016/s0022-3476(60)80186-2.
EISNER, V., PAULI, L. L., & LIVINGSTON, S. (1960). Epilepsy in the families of epileptics. The Journal of pediatrics, 56347-54. https://doi.org/10.1016/s0022-3476(60)80186-2
EISNER, V, et al. "Epilepsy in the families of epileptics." The Journal of pediatrics vol. 56 (1960): 347-54. doi: https://doi.org/10.1016/s0022-3476(60)80186-2
EISNER V, PAULI LL, LIVINGSTON S. Epilepsy in the families of epileptics. J Pediatr. 1960 Mar;56:347-54. doi: 10.1016/s0022-3476(60)80186-2. PMID: 13819783.
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[Possibility for genetic diagnosis of epilepsy].

Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica

Kaneko T, Kanei K.
PMID: 15307282
Seishin Shinkeigaku Zasshi. 2004;106(5):660-70.

No abstract available.

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Kaneko T, Kanei K. [Possibility for genetic diagnosis of epilepsy]. Seishin Shinkeigaku Zasshi. 2004;106(5):660-70
Kaneko, T., & Kanei, K. (2004). [Possibility for genetic diagnosis of epilepsy]. Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica, 106(5), 660-70.
Kaneko, Tadashi, and Kanei, Kazuaki. "[Possibility for genetic diagnosis of epilepsy]." Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica vol. 106,5 (2004): 660-70.
Kaneko T, Kanei K. [Possibility for genetic diagnosis of epilepsy]. Seishin Shinkeigaku Zasshi. 2004;106(5):660-70. PMID: 15307282.
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Introduction: Epilepsy at the cutting edge: a meeting in honor of Fred and Eva Andermann.

Epilepsia

Gotman J, Dubeau F.
PMID: 20331701
Epilepsia. 2010 Feb;51:1-2. doi: 10.1111/j.1528-1167.2009.02431.x.

No abstract available.

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Gotman J, Dubeau F. Introduction: Epilepsy at the cutting edge: a meeting in honor of Fred and Eva Andermann. Epilepsia. 2010;51:1-2doi: 10.1111/j.1528-1167.2009.02431.x.
Gotman, J., & Dubeau, F. (2010). Introduction: Epilepsy at the cutting edge: a meeting in honor of Fred and Eva Andermann. Epilepsia, 511-2. https://doi.org/10.1111/j.1528-1167.2009.02431.x
Gotman, Jean, and Dubeau, François. "Introduction: Epilepsy at the cutting edge: a meeting in honor of Fred and Eva Andermann." Epilepsia vol. 51 (2010): 1-2. doi: https://doi.org/10.1111/j.1528-1167.2009.02431.x
Gotman J, Dubeau F. Introduction: Epilepsy at the cutting edge: a meeting in honor of Fred and Eva Andermann. Epilepsia. 2010 Feb;51:1-2. doi: 10.1111/j.1528-1167.2009.02431.x. PMID: 20331701.
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The inheritance of epilepsy.

Pediatria de las Americas

NIETO D.
PMID: 21027179
Pediatr Am. 1946 Apr;4:247-52.

No abstract available.

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NIETO D. La herencia de la epilepsia. The inheritance of epilepsy. Pediatr Am. 1946;4:247-52
NIETO, D. (1946). La herencia de la epilepsia. The inheritance of epilepsy. Pediatria de las Americas, 4247-52.
NIETO, D. "La herencia de la epilepsia." The inheritance of epilepsy. Pediatria de las Americas vol. 4 (1946): 247-52.
NIETO D. La herencia de la epilepsia. The inheritance of epilepsy. Pediatr Am. 1946 Apr;4:247-52. Spanish. PMID: 21027179.
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Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests.

Human heredity

Steffens M, Becker T, Sander T, Fimmers R, Herold C, Holler DA, Leu C, Herms S, Cichon S, Bohn B, Gerstner T, Griebel M, Nöthen MM, Wienker TF, Baur MP.
PMID: 20357478
Hum Hered. 2010;69(4):268-84. doi: 10.1159/000295896. Epub 2010 Mar 31.

The Genome-Wide Association Study (GWAS) is the study design of choice for detecting common genetic risk factors for multifactorial diseases. The performance of full Genome-Wide Interaction Analyses (GWIA) has always been considered computationally challenging. Two-stage strategies to reduce the...

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Steffens M, Becker T, Sander T, et al. Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests. Hum Hered. 2010;69(4):268-84doi: 10.1159/000295896.
Steffens, M., Becker, T., Sander, T., Fimmers, R., Herold, C., Holler, D. A., Leu, C., Herms, S., Cichon, S., Bohn, B., Gerstner, T., Griebel, M., Nöthen, M. M., Wienker, T. F., & Baur, M. P. (2010). Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests. Human heredity, 69(4), 268-84. https://doi.org/10.1159/000295896
Steffens, Michael, et al. "Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests." Human heredity vol. 69,4 (2010): 268-84. doi: https://doi.org/10.1159/000295896
Steffens M, Becker T, Sander T, Fimmers R, Herold C, Holler DA, Leu C, Herms S, Cichon S, Bohn B, Gerstner T, Griebel M, Nöthen MM, Wienker TF, Baur MP. Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests. Hum Hered. 2010;69(4):268-84. doi: 10.1159/000295896. Epub 2010 Mar 31. PMID: 20357478.
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[The leading edge of epilepsy research].

Rinsho shinkeigaku = Clinical neurology

Ikeda A.
PMID: 22277454
Rinsho Shinkeigaku. 2011 Nov;51(11):993-6. doi: 10.5692/clinicalneurol.51.993.

For diagnosis of seizure type and epilepsy syndrome, we always take all the three aspects of 1) history and symptoms (symptomatology), 2) EEG (clinical neurophysiology) and 3) neuroimaging into account, and thus an appropriate treatment approach based on both...

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Ikeda A. [The leading edge of epilepsy research]. Rinsho Shinkeigaku. 2011;51(11):993-6doi: 10.5692/clinicalneurol.51.993.
Ikeda, A. (2011). [The leading edge of epilepsy research]. Rinsho shinkeigaku = Clinical neurology, 51(11), 993-6. https://doi.org/10.5692/clinicalneurol.51.993
Ikeda, Akio. "[The leading edge of epilepsy research]." Rinsho shinkeigaku = Clinical neurology vol. 51,11 (2011): 993-6. doi: https://doi.org/10.5692/clinicalneurol.51.993
Ikeda A. [The leading edge of epilepsy research]. Rinsho Shinkeigaku. 2011 Nov;51(11):993-6. doi: 10.5692/clinicalneurol.51.993. Japanese. PMID: 22277454.
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Showing 1 to 12 of 81 entries