Results 101 to 110 of about 2,188 (120)

Acid sphingomyelinase deficiency with homozygous p.Arg610del genotype in an elderly patient: a rare case report. [PDF]

J Bras Pneumol
Bridi GDP, Kairalla RA, Sawamura MVY, Baldi BG.   +3 more
europepmc   +1 more source

Reduction of sphingomyelinase activity associated with progranulin deficiency and frontotemporal dementia. [PDF]

Neurobiol Dis
Boyle NR, Fox SN, Tadepalli AS, Seyfried NT, Kukar T, Ramos EM, Nana AL, Spina S, Grinberg LT, Miller BL, Seeley WW, Arrant AE, Roberson ED.   +12 more
europepmc   +1 more source

Identification of ferroptosis-related gene signatures in temporal lobe epilepsy with hippocampal sclerosis. [PDF]

Front Neurosci
Gao F, Li J.
europepmc   +1 more source

A Pair of Fluorescent Probes Enabling Precise Diagnosis of Liver Cancer by Complementary Imaging. [PDF]

ACS Cent Sci
Gao M, Lee SH, Kwon HY, Ciaramicoli LM, Jo E, Yu YH, Li F, Kim B, Hong K, Lee JS, Kim N, Oh Y, Im CY, Tan CSH, Ha HH, Chang YT.   +15 more
europepmc   +1 more source

Neurodegenerative Diseases in Children: A Comprehensive Review. [PDF]

Int J Mol Sci
Ailioaie C, Ailioaie LM, Stan CI, Sava A, Chiran DA.   +4 more
europepmc   +1 more source

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mRNA Expression of SMPD1 Encoding Acid Sphingomyelinase Decreases upon Antidepressant Treatment

International Journal of Molecular Sciences, 2021
Tanja Richter-Schmidinger, Bernd Lenz, Iulia Zoicas   +2 more
exaly  

SMPD1 gene variants in patients with β-Thalassemia major

Molecular Biology Reports, 2023
Filiz Özen, Fadime Ersoy Dursun
exaly  

The emerging role of SMPD1 mutations in Parkinson's disease: Implications for future studies

Parkinsonism and Related Disorders, 2015
Guy A Rouleau, Avi Orr-Urtreger, Susan Bressman   +2 more
exaly  

The contribution of Niemann-Pick SMPD1 mutations to Parkinson disease in Ashkenazi Jews

Parkinsonism and Related Disorders, 2015
R Gershoni-Baruch
exaly