107 related articles for article (PubMed ID: 6476009)
1. Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly.
Dobyns WB; Stratton RF; Greenberg F
Am J Med Genet; 1984 Jul; 18(3):509-26. PubMed ID: 6476009
[TBL] [Abstract][Full Text] [Related]
2. Histopathologic Findings Associated with Miller-Dieker Syndrome: An Autopsy Report.
Bahmad HF; Ramesar L; Nosti C; Anthonio G; Brathwaite C; Vincentelli C; Castellano-Sánchez AA; Poppiti R
Diseases; 2022 Nov; 10(4):. PubMed ID: 36412589
[TBL] [Abstract][Full Text] [Related]
3. RETRACTED: Bahmad et al. Histopathologic Findings Associated with Miller-Dieker Syndrome: An Autopsy Report.
Bahmad HF; Ramesar L; Nosti C; Anthonio G; Brathwaite C; Vincentelli C; Castellano-Sánchez AA; Poppiti R
Diseases; 2023 Dec; 12(1):. PubMed ID: 38275567
[TBL] [Abstract][Full Text] [Related]
4. Child Neurology: RNA Sequencing for the Diagnosis of Lissencephaly.
Qashqari H; Ramani A; Gonorazky H; Amburgey K; Ghahramani Seno MM; Brudno M; Naumenko S; Das S; Dowling JJ
Neurology; 2021 Sep; 97(12):e1253-e1256. PubMed ID: 34016710
[No Abstract] [Full Text] [Related]
5. Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats.
Reiner O; Carrozzo R; Shen Y; Wehnert M; Faustinella F; Dobyns WB; Caskey CT; Ledbetter DH
Nature; 1993 Aug; 364(6439):717-21. PubMed ID: 8355785
[TBL] [Abstract][Full Text] [Related]
6. Total callosotomy ameliorates epileptic activity and improves cognitive function in a patient with Miller-Dieker syndrome.
Fukuoka M; Kuki I; Hattori Y; Tsuji H; Horino A; Nukui M; Inoue T; Okazaki S; Kunihiro N; Uda T
Epilepsy Behav Rep; 2024; 26():100670. PubMed ID: 38725538
[TBL] [Abstract][Full Text] [Related]
7. Brain Pathways in LIS1-Associated Lissencephaly Revealed by Diffusion MRI Tractography.
Ortug A; Valli B; Alatorre Warren JL; Shiohama T; van der Kouwe A; Takahashi E
Brain Sci; 2023 Nov; 13(12):. PubMed ID: 38137102
[TBL] [Abstract][Full Text] [Related]
8. Acute Bowel Ischemia in a Premature Neonate with Miller-Dieker Syndrome and Anomalous Right Coronary Artery From the Pulmonary Artery.
Cera AJ; Mokha S; Sunderji S; Cortez D; Bautista GM
Pediatr Ann; 2023 Aug; 52(8):e283-e291. PubMed ID: 37561828
[TBL] [Abstract][Full Text] [Related]
9. From circuits to behavior: Amygdala dysfunction in fragile X syndrome.
Svalina MN; Sullivan R; Restrepo D; Huntsman MM
Front Integr Neurosci; 2023; 17():1128529. PubMed ID: 36969493
[TBL] [Abstract][Full Text] [Related]
10. Doublecortin and JIP3 are neural-specific counteracting regulators of dynein-mediated retrograde trafficking.
Fu X; Rao L; Li P; Liu X; Wang Q; Son AI; Gennerich A; Liu JS
Elife; 2022 Dec; 11():. PubMed ID: 36476638
[TBL] [Abstract][Full Text] [Related]
11. Genes and brain malformations associated with abnormal neuron positioning.
Moffat JJ; Ka M; Jung EM; Kim WY
Mol Brain; 2015 Nov; 8(1):72. PubMed ID: 26541977
[TBL] [Abstract][Full Text] [Related]
12. Cenpj/CPAP regulates progenitor divisions and neuronal migration in the cerebral cortex downstream of Ascl1.
Garcez PP; Diaz-Alonso J; Crespo-Enriquez I; Castro D; Bell D; Guillemot F
Nat Commun; 2015 Mar; 6():6474. PubMed ID: 25753651
[TBL] [Abstract][Full Text] [Related]
13. Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly.
Fallet-Bianco C; Laquerrière A; Poirier K; Razavi F; Guimiot F; Dias P; Loeuillet L; Lascelles K; Beldjord C; Carion N; Toussaint A; Revencu N; Addor MC; Lhermitte B; Gonzales M; Martinovich J; Bessieres B; Marcy-Bonnière M; Jossic F; Marcorelles P; Loget P; Chelly J; Bahi-Buisson N
Acta Neuropathol Commun; 2014 Jul; 2():69. PubMed ID: 25059107
[TBL] [Abstract][Full Text] [Related]
14. Unilateral closed lip schizencephaly with septo-optic dysplasia.
Bhatnagar S; Kuber R; Shah D; Kulkarni V
Ann Med Health Sci Res; 2014 Mar; 4(2):283-5. PubMed ID: 24761255
[TBL] [Abstract][Full Text] [Related]
15. The key gluconeogenic enzyme fructose-1,6-bisphosphatase is secreted during prolonged glucose starvation and is internalized following glucose re-feeding via the non-classical secretory and internalizing pathways in Saccharomyces cerevisiae.
Giardina BJ; Chiang HL
Plant Signal Behav; 2013 Aug; 8(8):. PubMed ID: 23673352
[TBL] [Abstract][Full Text] [Related]
16. Vid30 is required for the association of Vid vesicles and actin patches in the vacuole import and degradation pathway.
Alibhoy AA; Giardina BJ; Dunton DD; Chiang HL
Autophagy; 2012 Jan; 8(1):29-46. PubMed ID: 22082961
[TBL] [Abstract][Full Text] [Related]
17. Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].
Alkuraya FS; Cai X; Emery C; Mochida GH; Al-Dosari MS; Felie JM; Hill RS; Barry BJ; Partlow JN; Gascon GG; Kentab A; Jan M; Shaheen R; Feng Y; Walsh CA
Am J Hum Genet; 2011 May; 88(5):536-47. PubMed ID: 21529751
[TBL] [Abstract][Full Text] [Related]
18. Molecular genetics of neuronal migration disorders.
Liu JS
Curr Neurol Neurosci Rep; 2011 Apr; 11(2):171-8. PubMed ID: 21222180
[TBL] [Abstract][Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]