These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 37096266)

  • 21. [Clinical and genetic characteristics of focal epilepsy in children caused by GATOR1 complex gene variation].
    Deng J; Fang F; Wang XH; Dai LF; Tian XJ; Chen CH
    Zhonghua Er Ke Za Zhi; 2019 Oct; 57(10):780-785. PubMed ID: 31594065
    [No Abstract]   [Full Text] [Related]  

  • 22. A Patient With CAD Deficiency Responsive to Uridine and Literature Review.
    Zhou L; Xu H; Wang T; Wu Y
    Front Neurol; 2020; 11():64. PubMed ID: 32117025
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical features and surgical outcomes in young children with focal cortical dysplasia type II.
    Wang TS; Liu QZ; Liu M; Zhang Q; Wang RF; Wu CW; Zhang J; Wang W; Ji TY; Liu XY; Wang S; Cai LX; Jiang YW; Wu Y
    CNS Neurosci Ther; 2020 Feb; 26(2):270-277. PubMed ID: 31368639
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Uridine-responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings.
    McGraw CM; Mahida S; Jayakar P; Koh HY; Taylor A; Resnick T; Rodan L; Schwartz MA; Ejaz A; Sankaran VG; Berry G; Poduri A
    Ann Clin Transl Neurol; 2021 Mar; 8(3):716-722. PubMed ID: 33497533
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Early onset epileptic encephalopathy caused by mitochondrial arginyl-tRNA synthetase gene deficiency: report of two cases and literature review].
    Jiang HF; Deng J; Fang F; Li H; Wang XH; Dai LF
    Zhonghua Er Ke Za Zhi; 2020 Nov; 58(11):893-899. PubMed ID: 33120460
    [No Abstract]   [Full Text] [Related]  

  • 26. [Genetic and clinical analysis of children with early-onset epilepsy encephalopathy caused by KCNT1 gene mutation].
    Chen Y; Bao XH; Zhang QP; Wang JP; Wen YX; Yu SJ; Zhao Y
    Zhonghua Er Ke Za Zhi; 2018 Nov; 56(11):824-828. PubMed ID: 30392206
    [No Abstract]   [Full Text] [Related]  

  • 27. [DNM1L gene variant caused encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1: three cases report and literature review].
    Pan Z; Wu TH; Chen C; Peng P; He YW; Yi WZ; Yin F; Peng J
    Zhonghua Er Ke Za Zhi; 2021 May; 59(5):400-406. PubMed ID: 33902225
    [No Abstract]   [Full Text] [Related]  

  • 28. Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the
    Barba C; Blumcke I; Winawer MR; Hartlieb T; Kang HC; Grisotto L; Chipaux M; Bien CG; Heřmanovská B; Porter BE; Lidov HGW; Cetica V; Woermann FG; Lopez-Rivera JA; Canoll PD; Mader I; D'Incerti L; Baldassari S; Yang E; Gaballa A; Vogel H; Straka B; Macconi L; Polster T; Grant GA; Krsková L; Shin HJ; Ko A; Crino PB; Krsek P; Lee JH; Lal D; Baulac S; Poduri A; Guerrini R;
    Neurology; 2023 Jan; 100(5):e528-e542. PubMed ID: 36307217
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Clinical features of epilepsy in 5 children with Mowat-Wilson syndrome].
    Ju Y; Ji TY
    Zhonghua Er Ke Za Zhi; 2022 Jun; 60(6):578-582. PubMed ID: 35658366
    [No Abstract]   [Full Text] [Related]  

  • 30. [Analysis of clinical and imaging features of 6 cases of linear scleroderma en coup de sabre with central nervous system involvement in children].
    Zhuo XW; Fang F; Gong S; Feng WX; Ding CH; Xiang X; Ge M; Zhang N; Li JW
    Zhonghua Er Ke Za Zhi; 2022 Nov; 60(11):1147-1152. PubMed ID: 36319148
    [No Abstract]   [Full Text] [Related]  

  • 31. Epilepsy in children with methylmalonic acidemia: electroclinical features and prognosis.
    Ma X; Zhang Y; Yang Y; Liu X; Yang Z; Bao X; Qin J; Wu X
    Brain Dev; 2011 Oct; 33(9):790-5. PubMed ID: 21764232
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
    Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
    Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Generation of a human iPSC line BCHNCi001-A from a patient with uridine-responsive epileptic encephalopathy carrying biallelic CAD mutations.
    Zhou L; Xu H; Wu Y; Fang F
    Stem Cell Res; 2022 Dec; 65():102947. PubMed ID: 36283272
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Seizure features and outcomes in 50 children with GATOR1 variants: A retrospective study, more favorable for epilepsy surgery.
    Wang H; Liu W; Zhang Y; Liu Q; Cai L; Jiang Y
    Epilepsia Open; 2023 Sep; 8(3):969-979. PubMed ID: 37259768
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Clinical characteristics of SLC35A2 gene variants related congenital disorders of glycosylation typeⅡ].
    Lang CH; Yang Y; Niu XY; Yang XL; Chen Y; Zhang YH
    Zhonghua Er Ke Za Zhi; 2020 Jul; 58(7):586-590. PubMed ID: 32605344
    [No Abstract]   [Full Text] [Related]  

  • 36. [Clinical phenotypes of TBC1D24 gene related epilepsy].
    Zhang J; Zhang YH; Chen JY; Zhang LP; Zeng Q; Tian XJ; Yang ZX; Wu Y; Yang XL; Wu XR
    Zhonghua Er Ke Za Zhi; 2018 Sep; 56(9):667-673. PubMed ID: 30180405
    [No Abstract]   [Full Text] [Related]  

  • 37. [Analysis of clinical and genetic characteristics of epilepsy associated with chromosome 16p11.2 microdeletion].
    Wang HS; Deng J; Wang XH; Chen CH; Wang X; Zhuo XW; Dai LF; Li H; Fang F
    Zhonghua Er Ke Za Zhi; 2022 Apr; 60(4):339-344. PubMed ID: 35385941
    [No Abstract]   [Full Text] [Related]  

  • 38. PIGN encephalopathy: Characterizing the epileptology.
    Bayat A; de Valles-Ibáñez G; Pendziwiat M; Knaus A; Alt K; Biamino E; Bley A; Calvert S; Carney P; Caro-Llopis A; Ceulemans B; Cousin J; Davis S; des Portes V; Edery P; England E; Ferreira C; Freeman J; Gener B; Gorce M; Heron D; Hildebrand MS; Jezela-Stanek A; Jouk PS; Keren B; Kloth K; Kluger G; Kuhn M; Lemke JR; Li H; Martinez F; Maxton C; Mefford HC; Merla G; Mierzewska H; Muir A; Monfort S; Nicolai J; Norman J; O'Grady G; Oleksy B; Orellana C; Orec LE; Peinhardt C; Pronicka E; Rosello M; Santos-Simarro F; Schwaibold EMC; Stegmann APA; Stumpel CT; Szczepanik E; Terczyńska I; Thevenon J; Tzschach A; Van Bogaert P; Vittorini R; Walsh S; Weckhuysen S; Weissman B; Wolfe L; Reymond A; De Nittis P; Poduri A; Olson H; Striano P; Lesca G; Scheffer IE; Møller RS; Sadleir LG
    Epilepsia; 2022 Apr; 63(4):974-991. PubMed ID: 35179230
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Clinical characteristics of PCDH19-female limited epilepsy].
    Chen Y; Yang XL; Liu AJ; Sun D; Yang Y; Zhang J; Chen JY; Yang ZX; Jiang YW; Wu XR; Zhang YH
    Zhonghua Er Ke Za Zhi; 2019 Nov; 57(11):857-862. PubMed ID: 31665840
    [No Abstract]   [Full Text] [Related]  

  • 40. [Clinical and genetic spectrum of SCN2A gene associated epilepsy and episodic ataxia].
    Guan J; Du KX; Dong Y; Li L; Song PP; Gong H; Zhang XL; Jia TM
    Zhonghua Er Ke Za Zhi; 2022 Jan; 60(1):51-55. PubMed ID: 34986624
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.