140 related articles for article (PubMed ID: 32045939)
21. Three patients manifesting early infantile epileptic spasms associated with 2q24.3 microduplications.
Yoshitomi S; Takahashi Y; Ishizuka M; Yamaguchi T; Watanabe A; Nasu H; Ueda Y; Ohtani H; Ikeda H; Imai K; Shigematsu H; Inoue Y; Tanahashi Y; Aiba K; Ohta H; Shimada S; Yamamoto T
Brain Dev; 2015 Oct; 37(9):874-9. PubMed ID: 25843248
[TBL] [Abstract][Full Text] [Related]
22. Infantile epileptic encephalopathy with hypsarrhythmia (infantile spasms/West syndrome).
Hrachovy RA; Frost JD
J Clin Neurophysiol; 2003; 20(6):408-25. PubMed ID: 14734931
[TBL] [Abstract][Full Text] [Related]
23. A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiency.
Barcia G; Barnerias C; Rio M; Siquier-Pernet K; Desguerre I; Colleaux L; Munnich A; Rotig A; Nabbout R
Eur J Med Genet; 2013 Dec; 56(12):683-5. PubMed ID: 24095819
[TBL] [Abstract][Full Text] [Related]
24. [Early-onset epileptic encephalopathy caused by CDKL5 mutation].
Hjalmgrim H; Hansen LK; Ousager LB; Møller RS
Ugeskr Laeger; 2014 Dec; 176(25A):. PubMed ID: 25497626
[TBL] [Abstract][Full Text] [Related]
25. Novel STXBP1 mutations in 2 patients with early infantile epileptic encephalopathy.
Sampaio M; Rocha R; Biskup S; Leão M
J Child Neurol; 2015 Apr; 30(5):622-4. PubMed ID: 23533165
[TBL] [Abstract][Full Text] [Related]
26. The Expanding Clinical Spectrum of Genetic Pediatric Epileptic Encephalopathies.
Shbarou R; Mikati MA
Semin Pediatr Neurol; 2016 May; 23(2):134-42. PubMed ID: 27544470
[TBL] [Abstract][Full Text] [Related]
27. Benign spasms of infancy: a mimicker of infantile epileptic disorders.
Ghossein J; Pohl D
Epileptic Disord; 2019 Dec; 21(6):585-589. PubMed ID: 31843733
[TBL] [Abstract][Full Text] [Related]
28. Two Japanese cases of epileptic encephalopathy associated with an FGF12 mutation.
Takeguchi R; Haginoya K; Uchiyama Y; Fujita A; Nagura M; Takeshita E; Inui T; Okubo Y; Sato R; Miyabayashi T; Togashi N; Saito T; Nakagawa E; Sugai K; Nakashima M; Saitsu H; Matsumoto N; Sasaki M
Brain Dev; 2018 Sep; 40(8):728-732. PubMed ID: 29699863
[TBL] [Abstract][Full Text] [Related]
29. The phenotypic spectrum of X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy.
Datta AN; Bahi-Buisson N; Bienvenu T; Buerki SE; Gardiner F; Cross JH; Heron B; Kaminska A; Korff CM; Lepine A; Lesca G; McTague A; Mefford HC; Mignot C; Milh M; Piton A; Pressler RM; Ruf S; Sadleir LG; de Saint Martin A; Van Gassen K; Verbeek NE; Ville D; Villeneuve N; Zacher P; Scheffer IE; Lemke JR
Epilepsia; 2021 Feb; 62(2):325-334. PubMed ID: 33410528
[TBL] [Abstract][Full Text] [Related]
30. Quinidine therapy for West syndrome with KCNTI mutation: A case report.
Fukuoka M; Kuki I; Kawawaki H; Okazaki S; Kim K; Hattori Y; Tsuji H; Nukui M; Inoue T; Yoshida Y; Uda T; Kimura S; Mogami Y; Suzuki Y; Okamoto N; Saitsu H; Matsumoto N
Brain Dev; 2017 Jan; 39(1):80-83. PubMed ID: 27578169
[TBL] [Abstract][Full Text] [Related]
31. [Genetic causes of infantile spasms--a systematic review].
Hansen LK; Ousager LB; Møller RS; Uldall PV; Hjalgrim H
Ugeskr Laeger; 2012 Apr; 174(17):1152-5. PubMed ID: 22533931
[TBL] [Abstract][Full Text] [Related]
32. Early-onset infant epileptic encephalopathy associated with a de novo
Qian Y; Wu B; Lu Y; Dong X; Qin Q; Zhou W; Wang H
Cold Spring Harb Mol Case Stud; 2018 Dec; 4(6):. PubMed ID: 30455226
[TBL] [Abstract][Full Text] [Related]
33. PRICKLE1-related early onset epileptic encephalopathy.
Mastrangelo M; Tolve M; Martinelli M; Di Noia SP; Parrini E; Leuzzi V
Am J Med Genet A; 2018 Dec; 176(12):2841-2845. PubMed ID: 30345727
[TBL] [Abstract][Full Text] [Related]
34. Atonic elements combined or uncombined with epileptic spasms in infantile spasms.
Xue J; Qian P; Li H; Yang H; Liu X; Zhang Y; Yang Z
Clin Neurophysiol; 2017 Jan; 128(1):220-226. PubMed ID: 27940146
[TBL] [Abstract][Full Text] [Related]
35. Infantile spasms and pigmentary mosaicism.
Hansen LK; Bygum A; Krogh LN
Epilepsia; 2010 Jul; 51(7):1317-8. PubMed ID: 20041939
[TBL] [Abstract][Full Text] [Related]
36. Expression and Transcriptional Regulation of Human ATP6V1A Gene in Gastric Cancers.
Wang P; Wang L; Sha J; Lou G; Lu N; Hang B; Mao JH; Zou X
Sci Rep; 2017 Jun; 7(1):3015. PubMed ID: 28592880
[TBL] [Abstract][Full Text] [Related]
37. High prevalence of genetic alterations in early-onset epileptic encephalopathies associated with infantile movement disorders.
Kobayashi Y; Tohyama J; Kato M; Akasaka N; Magara S; Kawashima H; Ohashi T; Shiraishi H; Nakashima M; Saitsu H; Matsumoto N
Brain Dev; 2016 Mar; 38(3):285-92. PubMed ID: 26482601
[TBL] [Abstract][Full Text] [Related]
38. West syndrome and other infantile epileptic encephalopathies--Indian hospital experience.
Kalra V; Gulati S; Pandey RM; Menon S
Brain Dev; 2002 Mar; 24(2):130-9. PubMed ID: 11891107
[TBL] [Abstract][Full Text] [Related]
39. Early infantile-onset Leigh syndrome complicated with infantile spasms associated with the m.9185 T > C variant in the MT-ATP6 gene: Expanding the clinical spectrum.
Takada R; Tozawa T; Kondo H; Kizaki Z; Kishita Y; Okazaki Y; Murayama K; Ohtake A; Chiyonobu T
Brain Dev; 2020 Jan; 42(1):69-72. PubMed ID: 31500933
[TBL] [Abstract][Full Text] [Related]
40. A de novo pathogenic variant in neuronal differentiation factor 2 in a Chinese patient with early infantile epileptic encephalopathy.
Poon JYY; Mok MTS; Ho SKL; Cheng SSW; Lo IFM; Luk HM
Clin Dysmorphol; 2024 Jul; 33(3):128-133. PubMed ID: 38818821
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
