BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Severino M, Geraldo AF, Utz N, Tortora D, Pogledic I, Klonowski W, Triulzi F, Arrigoni F, Mankad K, Leventer RJ, Mancini GMS, Barkovich JA, Lequin MH, Rossi A. Definitions and classification of malformations of cortical development: practical guidelines. Brain 2020;143:2874-94. [PMID: 32779696 DOI: 10.1093/brain/awaa174] [Cited by in Crossref: 67] [Cited by in F6Publishing: 71] [Article Influence: 33.5] [Reference Citation Analysis]
Number Citing Articles
1 Yi F, Zhang C, Zou Y, Li X, Li J, Deng L, Chen L, Chen Z. Three-Dimensional Crystal Vue Imaging technology assessment of Sylvian fissures at 20-32+6 weeks' normal gestation. Eur Radiol 2023;33:2358-66. [PMID: 36385228 DOI: 10.1007/s00330-022-09253-w] [Reference Citation Analysis]
2 Straka B, Vlčková M, Libá Z, Heřmanovská B, Kynčl M, Dorňáková J, Táborský J, Kršek P, Musilová A, Janota J, Balaščaková M. COL4A1 mutation-related disorder presenting as fetal intracranial bleeding, hydrocephalus, and polymicrogyria. Epilepsia Open 2023;8:211-6. [PMID: 36504316 DOI: 10.1002/epi4.12681] [Reference Citation Analysis]
3 Luhmann HJ. Malformations-related neocortical circuits in focal seizures. Neurobiol Dis 2023;178:106018. [PMID: 36706927 DOI: 10.1016/j.nbd.2023.106018] [Reference Citation Analysis]
4 Bongers JJ, Gutierrez-Quintana R, Hammond G, José-López R. Clinical and MRI findings of a suspected cortical malformation presented as a giant cerebral pseudomass in a German Shepherd dog. Clin Case Rep 2023;11:e7057. [PMID: 36911639 DOI: 10.1002/ccr3.7057] [Reference Citation Analysis]
5 Rakhmatova RA, Nabiev ZN, Shamsov BA, Zoirov SR. Factors and prevalence of congenital malformations in the Republic of Tajikistan. jour 2023. [DOI: 10.52888/0514-2515-2022-355-4-64-70] [Reference Citation Analysis]
6 Liu W, Zhang H, Hu X, Zhou D, Wu X. Localized activity alternations in periventricular nodular heterotopia-related epilepsy. CNS Neurosci Ther 2023. [PMID: 36740260 DOI: 10.1111/cns.14104] [Reference Citation Analysis]
7 Fileva N, Severino M, Tortora D, Ramaglia A, Paladini D, Rossi A. Second trimester fetal MRI of the brain: Through the ground glass. J Clin Ultrasound 2023;51:283-99. [PMID: 36785503 DOI: 10.1002/jcu.23423] [Reference Citation Analysis]
8 Passaro EA. Neuroimaging in Adults and Children With Epilepsy. Continuum (Minneap Minn) 2023;29:104-55. [PMID: 36795875 DOI: 10.1212/CON.0000000000001242] [Reference Citation Analysis]
9 Brock S, Laquerriere A, Marguet F, Myers SJ, Hongjie Y, Baralle D, Vanderhasselt T, Stouffs K, Keymolen K, Kim S, Allen J, Shaulsky G, Chelly J, Marcorelle P, Aziza J, Villard L, Sacaze E, de Wit MCY, Wilke M, Mancini GMS, Hehr U, Lim D, Mansour S, Traynelis SF, Beneteau C, Denis-Musquer M, Jansen AC, Fry AE, Bahi-Buisson N. Overlapping cortical malformations in patients with pathogenic variants in GRIN1 and GRIN2B. J Med Genet 2023;60:183-92. [PMID: 35393335 DOI: 10.1136/jmedgenet-2021-107971] [Reference Citation Analysis]
10 Liu PC, Chen HH, Chou CC, Chen CJ, Chen YH, Lin CF, Chen C, Yu HY, Lee CC. Stereo-EEG for Epileptogenic Focus Localization in Schizencephaly: A Single-center Experience in Four Patients. World Neurosurg 2023:S1878-8750(23)00024-4. [PMID: 36632895 DOI: 10.1016/j.wneu.2023.01.019] [Reference Citation Analysis]
11 Falcicchio G, Riva A, La Neve A, Iacomino M, Lastella P, Suppressa P, Sciruicchio V, Trojano M, Striano P. Case report: LAMC3-associated cortical malformations: Case report of a novel stop-gain variant and literature review. Front Genet 2022;13:990350. [PMID: 36685914 DOI: 10.3389/fgene.2022.990350] [Reference Citation Analysis]
12 Zhang X, Xiao N, Cao Y, Peng Y, Lian A, Chen Y, Wang P, Gu W, Xiao B, Yu J, Wang H, Shu L. De novo variants in MAST4 related to neurodevelopmental disorders with developmental delay and infantile spasms: Genotype-phenotype association. Front Mol Neurosci 2023;16:1097553. [PMID: 36910266 DOI: 10.3389/fnmol.2023.1097553] [Reference Citation Analysis]
13 Ahmad S, Wu Y, Wu Z, Thung KH, Liu S, Lin W, Li G, Wang L, Yap PT. Multifaceted atlases of the human brain in its infancy. Nat Methods 2023;20:55-64. [PMID: 36585454 DOI: 10.1038/s41592-022-01703-z] [Reference Citation Analysis]
14 Zhang S, Luo Y, Zhao Y, Zhu F, Jiang X, Wang X, Mo T, Zeng H. Prognostic analysis in children with focal cortical dysplasia II undergoing epilepsy surgery: Clinical and radiological factors. Front Neurol 2023;14:1123429. [PMID: 36949857 DOI: 10.3389/fneur.2023.1123429] [Reference Citation Analysis]
15 Matsuzawa N, Poon LC, Machida M, Nakamura T, Uenishi K, Wah YM, Moungmaithong S, Itakura A, Chiyo H, Pooh RK. Cat‐Ear‐Line. J of Ultrasound Medicine 2022. [DOI: 10.1002/jum.16153] [Reference Citation Analysis]
16 Rossetti AC, Fechtner O, Maillard C, Hoffrichter A, Zillich L, Poisel E, Jabali A, Marsoner F, Wilkens R, Francis F, Bahi-buisson N, Koch P, Ladewig J. Capturing the pathomechanisms of different disease severities in a human cerebral organoid model of LIS1-lissencephaly.. [DOI: 10.1101/2022.12.19.520907] [Reference Citation Analysis]
17 Tolezano GC, Bastos GC, da Costa SS, Freire BL, Homma TK, Honjo RS, Yamamoto GL, Passos-bueno MR, Koiffmann CP, Kim CA, Vianna-morgante AM, de Lima Jorge AA, Bertola DR, Rosenberg C, Krepischi ACV. Burden of Rare Copy Number Variants in Microcephaly: A Brazilian Cohort of 185 Microcephalic Patients and Review of the Literature. J Autism Dev Disord 2022. [DOI: 10.1007/s10803-022-05853-z] [Reference Citation Analysis]
18 Gökçe E, Beyhan M, Ocak Karataş ŞF. Magnetic resonance imaging findings of two cases with West syndrome and hypomelanosis of Ito with hemimegalencephaly: a report of two cases. Egypt J Radiol Nucl Med 2022;53:136. [DOI: 10.1186/s43055-022-00809-w] [Reference Citation Analysis]
19 Khalaf-Nazzal R, Fasham J, Inskeep KA, Blizzard LE, Leslie JS, Wakeling MN, Ubeyratna N, Mitani T, Griffith JL, Baker W, Al-Hijawi F, Keough KC, Gezdirici A, Pena L, Spaeth CG, Turnpenny PD, Walsh JR, Ray R, Neilson A, Kouranova E, Cui X, Curiel DT, Pehlivan D, Akdemir ZC, Posey JE, Lupski JR, Dobyns WB, Stottmann RW, Crosby AH, Baple EL. Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder. Am J Hum Genet 2022;109:2068-79. [PMID: 36283405 DOI: 10.1016/j.ajhg.2022.09.012] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Lai A, Soucy A, El Achkar CM, Barkovich AJ, Cao Y, DiStefano M, Evenson M, Guerrini R, Knight D, Lee YS, Mefford HC, Miller DT, Mirzaa G, Mochida G, Rodan LH, Patel M, Smith L, Spencer S, Walsh CA, Yang E, Yuskaitis CJ, Yu T, Poduri A; ClinGen Brain Malformation Variant Curation Expert Panel. The ClinGen Brain Malformation Variant Curation Expert Panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2. Genet Med 2022;24:2240-8. [PMID: 35997716 DOI: 10.1016/j.gim.2022.07.020] [Reference Citation Analysis]
21 Gaines JJ, Gilbert BC, Gossage JR, Parker W, Reddy A, Forseen SE. Schizencephaly in Hereditary Hemorrhagic Telangiectasia. AJNR Am J Neuroradiol 2022;43:1603-7. [PMID: 36265891 DOI: 10.3174/ajnr.A7677] [Reference Citation Analysis]
22 Damianidou E, Mouratidou L, Kyrousi C. Research models of neurodevelopmental disorders: The right model in the right place. Front Neurosci 2022;16:1031075. [DOI: 10.3389/fnins.2022.1031075] [Reference Citation Analysis]
23 Straka B, Hermanovska B, Krskova L, Zamecnik J, Vlckova M, Balascakova M, Tesner P, Jezdik P, Tichy M, Kyncl M, Musilova A, Lassuthova P, Marusic P, Krsek P. Genetic Testing for Malformations of Cortical Development. Neurol Genet 2022;8:e200032. [DOI: 10.1212/nxg.0000000000200032] [Reference Citation Analysis]
24 Liu C, Liu Q, Yu H, Sun Y, Wang Y, Wang S, Ji T, Yu G, Wang W, Liu X, Jiang Y, Cai L. Subtotal hemispherotomy for intractable lesional hemispheric epilepsy without hemiparesis in children. Epilepsy Research 2022;185:106973. [DOI: 10.1016/j.eplepsyres.2022.106973] [Reference Citation Analysis]
25 Fasano G, Compagnucci C, Dallapiccola B, Tartaglia M, Lauri A. Teleost Fish and Organoids: Alternative Windows Into the Development of Healthy and Diseased Brains. Front Mol Neurosci 2022;15:855786. [DOI: 10.3389/fnmol.2022.855786] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
26 Maillard C, Roux CJ, Charbit-Henrion F, Steffann J, Laquerriere A, Quazza F, Buisson NB. Tubulin mutations in human neurodevelopmental disorders. Semin Cell Dev Biol 2022:S1084-9521(22)00238-5. [PMID: 35915025 DOI: 10.1016/j.semcdb.2022.07.009] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Holman R. Common Indications and Techniques in Prenatal MRI. Prenatal Diagnosis [Working Title] 2022. [DOI: 10.5772/intechopen.105361] [Reference Citation Analysis]
28 Amorosino G, Peruzzo D, Redaelli D, Olivetti E, Arrigoni F, Avesani P. DBB - A Distorted Brain Benchmark for Automatic Tissue Segmentation in Paediatric Patients. Neuroimage 2022;260:119486. [PMID: 35843515 DOI: 10.1016/j.neuroimage.2022.119486] [Reference Citation Analysis]
29 Kang H, Kim D, Kim SH, Lee JH, Ko A, Kim SH, Lee JS, Kim HD, Kang H. Epilepsy with SLC35A2 Brain Somatic Mutations in Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE). Ann Child Neurol 2022;30:88-94. [DOI: 10.26815/acn.2022.00073] [Reference Citation Analysis]
30 Xu H, Gao K, Liu Q, Wang T, Zhang Z, Cai L, Wu Y, Jiang Y. Brain Somatic Variant in Ras-Like Small GTPase RALA Causes Focal Cortical Dysplasia Type II. Front Behav Neurosci 2022;16:919485. [DOI: 10.3389/fnbeh.2022.919485] [Reference Citation Analysis]
31 Hasegawa D, Saito M, Kitagawa M. Neurosurgery in canine epilepsy. Vet J 2022;:105852. [PMID: 35716888 DOI: 10.1016/j.tvjl.2022.105852] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
32 Severino M, Tortora D, Reid C, Uccella S, Nobili L, Accogli A, Srour M, Ramaglia A, Sudhakar S, Consales A, Pavanello M, Piatelli G, James G, Ravegnani M, Rossi A, Mankad K. Imaging characteristics and neurosurgical outcome in subjects with agenesis of the corpus callosum and interhemispheric cysts. Neuroradiology 2022. [PMID: 35670822 DOI: 10.1007/s00234-022-02990-1] [Reference Citation Analysis]
33 Hauptman AJ, Barkoudah E. [The role of neuropsychiatry in the care of children and adults with cerebral palsy]. BJPsych Open 2022;8:e99. [PMID: 35642355 DOI: 10.1192/bjo.2022.62] [Reference Citation Analysis]
34 Abe K, Ando K, Kato M, Saitsu H, Nakashima M, Aoki S, Kimura T. A New Case With Cortical Malformation Caused by Biallelic Variants in LAMC3. Neurol Genet 2022;8:e680. [PMID: 35620139 DOI: 10.1212/NXG.0000000000000680] [Reference Citation Analysis]
35 Eroğlu Y, Ağlamiş S. Gri Cevher Heterotopisi Bulunan Pediatrik Hastaların Manyetik Rezonans Görüntüleme Bulguları ve Eşlik Eden Malformasyonların Değerlendirilmesi. KSÜ Tıp Fak Der 2022. [DOI: 10.17517/ksutfd.1023811] [Reference Citation Analysis]
36 Alves IS, Coutinho AMN, Vieira APF, Rocha BP, Passos UL, Gonçalves VT, Silva PDS, Zhan MX, Pinho PC, Delgado DS, Docema MFL, Lee HW, Policeni BA, Leite CC, Martin MGM, Amancio CT. Imaging Aspects of the Hippocampus. Radiographics 2022;42:822-40. [PMID: 35213261 DOI: 10.1148/rg.210153] [Reference Citation Analysis]
37 Barkovich MJ. Pediatric Brain Maturation and Migration Disorders. Diagnostics 2022;12:1123. [DOI: 10.3390/diagnostics12051123] [Reference Citation Analysis]
38 Pooh RK, Machida M, Matsuzawa N. Fetal Brain Structure and CNS Anomalies. Donald School Journal of Ultrasound in Obstetrics and Gynecology 2022;16:31-52. [DOI: 10.5005/jp-journals-10009-1921] [Reference Citation Analysis]
39 Lapalme-Remis S, Nguyen DK. Neuroimaging of Epilepsy. Continuum (Minneap Minn) 2022;28:306-38. [PMID: 35393961 DOI: 10.1212/CON.0000000000001080] [Reference Citation Analysis]
40 Ahmad S, Wu Y, Wu Z, Thung K, Lin W, Li G, Wang L, Yap P. Multifaceted Atlases of the Human Brain in its Infancy.. [DOI: 10.1101/2022.03.19.484985] [Reference Citation Analysis]
41 Rijckmans E, Stouffs K, Jansen AC, Brock S. Malformations of cerebral development and clues from the peripheral nervous system: A systematic literature review. Eur J Paediatr Neurol 2022;37:155-64. [PMID: 34535379 DOI: 10.1016/j.ejpn.2021.08.006] [Reference Citation Analysis]
42 Fischer J, Di Donato N. Diagnostic pitfalls in patients with malformations of cortical development. Eur J Paediatr Neurol 2022;37:123-8. [PMID: 35228169 DOI: 10.1016/j.ejpn.2022.01.017] [Reference Citation Analysis]
43 Simmons R, Martinez AB, Barkovich J, Numis AL, Cilio MR, Glenn OA, Gano D, Rogers EE, Glass HC. Disorders of Neuronal Migration/Organization Convey the Highest Risk of Neonatal Onset Epilepsy Compared With Other Congenital Brain Malformations. Pediatr Neurol 2022;127:20-7. [PMID: 34933271 DOI: 10.1016/j.pediatrneurol.2021.11.005] [Reference Citation Analysis]
44 Ossola C, Kalebic N. Roots of the Malformations of Cortical Development in the Cell Biology of Neural Progenitor Cells. Front Neurosci 2021;15:817218. [PMID: 35069108 DOI: 10.3389/fnins.2021.817218] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
45 Eroglu Y, Tuncer Kara K. Comparative Evaluation of Apparent Diffusion Coefficient Values of White Matter Surrounding the Heterotopia in Children With Unilateral Subependymal Heterotopia. Cureus 2022. [DOI: 10.7759/cureus.21458] [Reference Citation Analysis]
46 Muh CR. Hemispherectomy. Pediatric Neurosurgery for Clinicians 2022. [DOI: 10.1007/978-3-030-80522-7_40] [Reference Citation Analysis]
47 Boluda S, Seilhean D, Bielle F. Neuropathology of the temporal lobe. Handbook of Clinical Neurology 2022. [DOI: 10.1016/b978-0-12-823493-8.00027-4] [Reference Citation Analysis]
48 Schonstedt Geldres V, Stecher Guzmán X, Manterola Mordojovich C, Rovira À. Imaging in the study of macrocephaly: Why?, when?, how? Radiología (English Edition) 2022;64:26-40. [DOI: 10.1016/j.rxeng.2021.09.008] [Reference Citation Analysis]
49 Schonstedt Geldres V, Stecher Guzmán X, Manterola Mordojovich C, Rovira À. Radiología en el estudio de la macrocefalia. ¿Por qué?, ¿cuándo?, ¿cómo? Radiología 2022;64:26-40. [DOI: 10.1016/j.rx.2021.09.006] [Reference Citation Analysis]
50 Subramanian S, Biswas A, Alves CAPF, Sudhakar SV, Shekdar KV, Krishnan P, Shroff M, Taranath A, Arrigoni F, Aldinger KA, Leventer RJ, Dobyns WB, Mankad K. ACTA2-Related Dysgyria: An Under-Recognized Malformation of Cortical Development. AJNR Am J Neuroradiol 2022;43:146-50. [PMID: 34857515 DOI: 10.3174/ajnr.A7364] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
51 Khandelwal A, Aggarwal A, Sharma A, Malik A, Bose A. MRI of Malformations of Cortical Development- A Comprehensive Review. World Neurosurg 2021:S1878-8750(21)01854-4. [PMID: 34896352 DOI: 10.1016/j.wneu.2021.12.011] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
52 Park K, Hoff KJ, Wethekam L, Stence N, Saenz M, Moore JK. Kinetically Stabilizing Mutations in Beta Tubulins Create Isotype-Specific Brain Malformations. Front Cell Dev Biol 2021;9:765992. [PMID: 34869359 DOI: 10.3389/fcell.2021.765992] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
53 Li H, Ji S, Dong B, Chen L. Seizure control after epilepsy surgery in early childhood: A systematic review and meta-analysis. Epilepsy Behav 2021;125:108369. [PMID: 34731717 DOI: 10.1016/j.yebeh.2021.108369] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
54 Vriend I, Oegema R. Genetic causes underlying grey matter heterotopia. Eur J Paediatr Neurol 2021;35:82-92. [PMID: 34666232 DOI: 10.1016/j.ejpn.2021.09.015] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
55 Pogledic I, Schwartz E, Bobić-Rasonja M, Mitter C, Baltzer P, Gruber GM, Milković-Periša M, Haberler C, Bettelheim D, Kasprian G, Judaš M, Prayer D, Jovanov-Milošević N. 3T MRI signal intensity profiles and thicknesses of transient zones in human fetal brain at mid-gestation. Eur J Paediatr Neurol 2021;35:67-73. [PMID: 34653829 DOI: 10.1016/j.ejpn.2021.09.014] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
56 Chiba E, Kimura Y, Shimizu-Motohashi Y, Miyagawa N, Ota M, Shigemoto Y, Ohnishi M, Nakaya M, Nakagawa E, Sasaki M, Sato N. Clinical and neuroimaging findings in patients with lissencephaly/subcortical band heterotopia spectrum: a magnetic resonance conventional and diffusion tensor study. Neuroradiology 2021. [PMID: 34693484 DOI: 10.1007/s00234-021-02836-2] [Reference Citation Analysis]
57 Moloney PB, Cavalleri GL, Delanty N. Epilepsy in the mTORopathies: opportunities for precision medicine. Brain Commun 2021;3:fcab222. [PMID: 34632383 DOI: 10.1093/braincomms/fcab222] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
58 Urbach H, Heers M, Altenmueller DM, Schulze-Bonhage A, Staack AM, Bast T, Reisert M, Schwarzwald R, Kaller CP, Huppertz HJ, Demerath T. "Within a minute" detection of focal cortical dysplasia. Neuroradiology 2021. [PMID: 34625834 DOI: 10.1007/s00234-021-02823-7] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
59 Recent Fetal Neurology: From Neurosonography to Neurosonogenetics. Donald School Journal of Ultrasound in Obstetrics and Gynecology 2021;15:229-239. [DOI: 10.5005/jp-journals-10009-1718] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
60 Havali C, Bako D. Çocuklarda Kortikal Gelişimsel Malformasyonlara Tanısal Yaklaşım: 36 Hastanın Klinik, Görüntüleme ve Laboratuvar Verileri. Turkish Journal of Pediatric Disease 2021. [DOI: 10.12956/tchd.899026] [Reference Citation Analysis]
61 Lerman-Sagie T, Pogledic I, Leibovitz Z, Malinger G. A practical approach to prenatal diagnosis of malformations of cortical development. Eur J Paediatr Neurol 2021;34:50-61. [PMID: 34390998 DOI: 10.1016/j.ejpn.2021.08.001] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
62 Liu Q, Ma J, Yu G, Zhang Q, Zhu Y, Wang R, Yu H, Liu C, Sun Y, Wang W, Wang S, Ji T, Li M, Liu X, Jiang Y, Cai L, Wu Y. Postoperative seizure and developmental outcomes of children with hemimegalencephaly and drug-resistant epilepsy. Seizure 2021;92:29-35. [PMID: 34416421 DOI: 10.1016/j.seizure.2021.08.006] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
63 Xydis VG, Giantsouli A, Styliara E, Alexiou GA, Nakou I, Astrakas LG, Argyropoulou MI. Subcortical Band Heterotopia Shows Increased Perfusion on Arterial Spin Labeling Maps. Can J Neurol Sci 2021;:1. [PMID: 34382534 DOI: 10.1017/cjn.2021.194] [Reference Citation Analysis]
64 Zaki MS, Accogli A, Mirzaa G, Rahman F, Mohammed H, Porras-Hurtado GL, Efthymiou S, Maqbool S, Shukla A, Vincent JB, Hussain A, Mir A, Beetz C, Leubauer A, Houlden H, Gleeson JG, Maroofian R. Pathogenic variants in PIDD1 lead to an autosomal recessive neurodevelopmental disorder with pachygyria and psychiatric features. Eur J Hum Genet 2021;29:1226-34. [PMID: 34163010 DOI: 10.1038/s41431-021-00910-0] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
65 Qian X, Liu X, Zhu Z, Wang S, Song X, Chen G, Wu J, Cao Y, Luan X, Tang H, Cao L. Variants in LAMC3 Causes Occipital Cortical Malformation. Front Genet 2021;12:616761. [PMID: 34354730 DOI: 10.3389/fgene.2021.616761] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
66 Nakamura T, Chiyo H. Neurosonographic Approach to Malformations of Cortical Development. Donald School Journal of Ultrasound in Obstetrics and Gynecology 2021;15:179-187. [DOI: 10.5005/jp-journals-10009-1699] [Reference Citation Analysis]
67 Kobow K, Baulac S, von Deimling A, Lee JH. Molecular diagnostics in drug-resistant focal epilepsy define new disease entities. Brain Pathol 2021;31:e12963. [PMID: 34196984 DOI: 10.1111/bpa.12963] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
68 Sokpor G, Kerimoglu C, Nguyen H, Pham L, Rosenbusch J, Wagener R, Nguyen HP, Fischer A, Staiger JF, Tuoc T. Loss of BAF Complex in Developing Cortex Perturbs Radial Neuronal Migration in a WNT Signaling-Dependent Manner. Front Mol Neurosci 2021;14:687581. [PMID: 34220450 DOI: 10.3389/fnmol.2021.687581] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
69 Liu X, Shen Q, Zheng G, Guo H, Lu X, Wang X, Yang X, Cao Z, Chen J. Gene and Phenotype Expansion of Unexplained Early Infantile Epileptic Encephalopathy. Front Neurol 2021;12:633637. [PMID: 34163418 DOI: 10.3389/fneur.2021.633637] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
70 Macdonald-Laurs E, Maixner WJ, Bailey CA, Barton SM, Mandelstam SA, Yuan-Mou Yang J, Warren AEL, Kean MJ, Francis P, MacGregor D, D'Arcy C, Wrennall JA, Davidson A, Pope K, Leventer RJ, Freeman JL, Wray A, Jackson GD, Harvey AS. One-Stage, Limited-Resection Epilepsy Surgery for Bottom-of-Sulcus Dysplasia. Neurology 2021;97:e178-90. [PMID: 33947776 DOI: 10.1212/WNL.0000000000012147] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
71 Moltoni G, Talenti G, Righini A. Brain fetal neuroradiology: a beginner's guide. Transl Pediatr 2021;10:1065-77. [PMID: 34012856 DOI: 10.21037/tp-20-293] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
72 Bobić-Rasonja M, Pogledić I, Mitter C, Štajduhar A, Milković-Periša M, Trnski S, Bettelheim D, Hainfellner JA, Judaš M, Prayer D, Jovanov-Milošević N. Developmental Differences Between the Limbic and Neocortical Telencephalic Wall: An Intrasubject Slice-Matched 3 T MRI-Histological Correlative Study in Humans. Cereb Cortex 2021;31:3536-50. [PMID: 33704445 DOI: 10.1093/cercor/bhab030] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
73 Yang X, Zhang X, Ma Y, Wang Z, Huang K, Liu G, Shen K, Zhu G, Wang T, Lv S, Zhang C, Yang H, Liu S. Abnormal Rat Cortical Development Induced by Ventricular Injection of rHMGB1 Mimics the Pathophysiology of Human Cortical Dysplasia. Front Cell Dev Biol 2021;9:634405. [PMID: 33748118 DOI: 10.3389/fcell.2021.634405] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
74 Klingler E, Francis F, Jabaudon D, Cappello S. Mapping the molecular and cellular complexity of cortical malformations. Science 2021;371:eaba4517. [PMID: 33479124 DOI: 10.1126/science.aba4517] [Cited by in Crossref: 33] [Cited by in F6Publishing: 33] [Article Influence: 16.5] [Reference Citation Analysis]
75 Ikawa A, Fujimoto A, Arai Y, Otsuki Y, Nozaki T, Baba S, Sato K, Enoki H. Case Report: Late-Onset Temporal Lobe Epilepsy Following Subarachnoid Hemorrhage: An Interplay Between Pre-existing Cortical Development Abnormality and Tissue Damage. Front Neurol 2021;12:599130. [PMID: 33633663 DOI: 10.3389/fneur.2021.599130] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
76 Sculier C, Taussig D, David O, Blustajn J, Ayoubian L, Bonheur J, Bulteau C, Chipaux M, Dorison N, Raffo E, Ferrand-Sorbets S, Dorfmüller G, Fohlen M. Focal polymicrogyria in children: Contribution of invasive explorations and epileptogenicity mapping in the surgical decision. Seizure 2021;86:19-28. [PMID: 33517238 DOI: 10.1016/j.seizure.2021.01.010] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
77 Bonduelle T, Hartlieb T, Baldassari S, Sim NS, Kim SH, Kang HC, Kobow K, Coras R, Chipaux M, Dorfmüller G, Adle-Biassette H, Aronica E, Lee JH, Blumcke I, Baulac S. Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE). Acta Neuropathol Commun 2021;9:3. [PMID: 33407896 DOI: 10.1186/s40478-020-01085-3] [Cited by in Crossref: 32] [Cited by in F6Publishing: 34] [Article Influence: 16.0] [Reference Citation Analysis]
78 Accogli A, Geraldo AF, Piccolo G, Riva A, Scala M, Balagura G, Salpietro V, Madia F, Maghnie M, Zara F, Striano P, Tortora D, Severino M, Capra V. Diagnostic Approach to Macrocephaly in Children. Front Pediatr 2021;9:794069. [PMID: 35096710 DOI: 10.3389/fped.2021.794069] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 4.5] [Reference Citation Analysis]
79 Markus F, Kannengießer A, Näder P, Atigbire P, Scholten A, Vössing C, Bültmann E, Korenke GC, Owczarek-Lipska M, Neidhardt J. A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects. J Hum Genet 2021;66:1159-67. [PMID: 34211111 DOI: 10.1038/s10038-021-00947-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
80 Geraldo AF, Rossi A, Severino M. Malformations of Cortical Development. Pediatric Neuroradiology 2021. [DOI: 10.1007/978-3-662-46258-4_6-1] [Reference Citation Analysis]
81 Kobow K, Jabari S, Pieper T, Kudernatsch M, Polster T, Woermann FG, Kalbhenn T, Hamer H, Rössler K, Mühlebner A, Spliet WGM, Feucht M, Hou Y, Stichel D, Korshunov A, Sahm F, Coras R, Blümcke I, von Deimling A. Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay. Acta Neuropathol 2020;140:881-91. [PMID: 32979071 DOI: 10.1007/s00401-020-02228-5] [Cited by in Crossref: 19] [Cited by in F6Publishing: 14] [Article Influence: 6.3] [Reference Citation Analysis]