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childhood brain atrophy相关文献:
Childhood-Onset Neurodegeneration with Brain Atrophy in Association with c.628G>A in UBTF Gene.
Gunasekaran PK, Laxmi V, Manjunathan S, Kumar A, Tiwari S, Saini L.
Indian J Pediatr. 2023 Aug;90(8):835. doi: 10.1007/s12098-023-04642-5. Epub 2023 May 10.
PMID:37162731
Childhood adiposity underlies numerous adult brain traits commonly attributed to midlife obesity.
Chiesa ST, Rader L, Garfield V, Foote I, Suri S, Davey Smith G, Hughes AD, Richardson TG.
Brain. 2025 Jan 7;148(1):133-142. doi: 10.1093/brain/awae198.
PMID:38889233
Brain Magnetic Resonance Imaging (MRI) in Spinal Muscular Atrophy: A Scoping Review.
Mugisha N, Oliveira-Carneiro A, Behlim T, Oskoui M.
J Neuromuscul Dis. 2023;10(4):493-503. doi: 10.3233/JND-221567.
PMID:37125560
Brain, cognition, and language development in spinal muscular atrophy type 1: a scoping review.
Masson R, Brusa C, Scoto M, Baranello G.
Dev Med Child Neurol. 2021 May;63(5):527-536. doi: 10.1111/dmcn.14798. Epub 2021 Jan 15.
PMID:33452688
Brain magnetic resonance imaging of patients with spinal muscular atrophy type 2 and 3.
Stam M, Tan HHG, Schmidt R, van den Heuvel MP, van den Berg LH, Wadman RI, van der Pol WL.
Neuroimage Clin. 2024;44:103708. doi: 10.1016/j.nicl.2024.103708. Epub 2024 Nov 14.
PMID:39577334
Cerebellar Atrophy in Adult Survivors of Childhood Cerebellar Tumor.
Ailion AS, King TZ, Wang L, Fox ME, Mao H, Morris RM, Crosson B.
J Int Neuropsychol Soc. 2016 May;22(5):501-11. doi: 10.1017/S1355617716000138. Epub 2016 Mar 8.
PMID:26954713
A case-control study on the driving factors of childhood brain volume loss: What pediatricians must explore.
Sungura R, Shirima G, Spitsbergen J, Mpolya E, Vianney JM.
PLoS One. 2022 Dec 30;17(12):e0276433. doi: 10.1371/journal.pone.0276433. eCollection 2022.
PMID:36584214
Structural brain abnormalities specific to childhood-onset schizophrenia identified by neuroimaging techniques.
Mehler C, Warnke A.
J Neural Transm (Vienna). 2002 Feb;109(2):219-34. doi: 10.1007/s007020200019.
PMID:12075863
Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis.
Guerrini R, Mei D, Kerti-Szigeti K, Pepe S, Koenig MK, Von Allmen G, Cho MT, McDonald K, Baker J, Bhambhani V, Powis Z, Rodan L, Nabbout R, Barcia G, Rosenfeld JA, Bacino CA, Mignot C, Power LH, Harris CJ, Marjanovic D, Møller RS, Hammer TB; DDD Study; Keski Filppula R, Vieira P, Hildebrandt C, Sacharow S; Undiagnosed Diseases Network; Maragliano L, Benfenati F, Lachlan K, Benneche A, Petit F, de Sainte Agathe JM, Hallinan B, Si Y, Wentzensen IM, Zou F, Narayanan V, Matsumoto N, Boncristiano A, la Marca G, Kato M, Anderson K, Barba C, Sturiale L, Garozzo D, Bei R; ATP6V1A collaborators; Masuelli L, Conti V, Novarino G, Fassio A.
Brain. 2022 Aug 27;145(8):2687-2703. doi: 10.1093/brain/awac145.
PMID:35675510
Brain structural changes in alternating hemiplegia of childhood using single-case voxel-based morphometry analysis.
Arizono E, Sato N, Shigemoto Y, Kimura Y, Chiba E, Maki H, Matsuda H, Takeshita E, Shimizu-Motohashi Y, Sasaki M, Saito K.
Int J Dev Neurosci. 2023 Nov;83(7):665-673. doi: 10.1002/jdn.10295. Epub 2023 Aug 21.
PMID:37604479
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