Search details
1.
Platelet mitochondrial activity and pesticide exposure in early Parkinson's disease.
Mov Disord
; 30(6): 862-6, 2015 May.
Article
in English
| MEDLINE | ID: mdl-25757798
2.
Distribution of hand function by age in individuals with Rett syndrome.
Ann Child Neurol Soc
; 1(3): 228-238, 2023 Sep.
Article
in English
| MEDLINE | ID: mdl-38496825
3.
Effects of endotracheal intubation and surfactant on a 3-channel neonatal electroencephalogram.
J Pediatr
; 161(2): 252-7, 2012 Aug.
Article
in English
| MEDLINE | ID: mdl-22424942
4.
A seven-day study of the pharmacokinetics of intravenous levetiracetam in neonates: marked changes in pharmacokinetics occur during the first week of life.
Pediatr Res
; 72(1): 43-9, 2012 Jul.
Article
in English
| MEDLINE | ID: mdl-22495532
5.
Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history study.
J Neurodev Disord
; 14(1): 31, 2022 05 14.
Article
in English
| MEDLINE | ID: mdl-35568815
6.
Quality improvement of mitochondrial respiratory chain complex enzyme assays using Caenorhabditis elegans.
Genet Med
; 13(9): 794-9, 2011 Sep.
Article
in English
| MEDLINE | ID: mdl-21633293
7.
Levetiracetam Versus Phenobarbital for Neonatal Seizures: A Randomized Controlled Trial.
Pediatrics
; 145(6)2020 06.
Article
in English
| MEDLINE | ID: mdl-32385134
8.
Determination of DNA mutation load in human tissues using denaturing HPLC-based heteroduplex analysis.
Methods Mol Biol
; 554: 287-99, 2009.
Article
in English
| MEDLINE | ID: mdl-19513681
9.
Mitochondrial Dysfunction in Aging and Diseases of Aging.
Biology (Basel)
; 8(2)2019 Jun 17.
Article
in English
| MEDLINE | ID: mdl-31213034
10.
11.
Impact of nucleoside reverse transcriptase inhibitors on mitochondrial DNA and RNA in human skeletal muscle cells.
Antimicrob Agents Chemother
; 52(8): 2825-30, 2008 Aug.
Article
in English
| MEDLINE | ID: mdl-18541728
12.
Pitfalls in the denaturing high-performance liquid chromatography analysis of mitochondrial DNA mutation.
J Mol Diagn
; 10(1): 102-8, 2008 Jan.
Article
in English
| MEDLINE | ID: mdl-18165269
13.
The in-depth evaluation of suspected mitochondrial disease.
Mol Genet Metab
; 94(1): 16-37, 2008 May.
Article
in English
| MEDLINE | ID: mdl-18243024
14.
Pontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidance.
Brain
; 130(Pt 9): 2258-66, 2007 Sep.
Article
in English
| MEDLINE | ID: mdl-17690130
15.
Paroxysmal motor disorders: expanding phenotypes lead to coalescing genotypes.
Ann Clin Transl Neurol
; 5(8): 996-1010, 2018 Aug.
Article
in English
| MEDLINE | ID: mdl-30128325
16.
Endocrine Disorders in Primary Mitochondrial Disease.
J Endocr Soc
; 2(4): 361-373, 2018 Apr 01.
Article
in English
| MEDLINE | ID: mdl-29594260
17.
The evidence basis for coenzyme Q therapy in oxidative phosphorylation disease.
Mitochondrion
; 7 Suppl: S136-45, 2007 Jun.
Article
in English
| MEDLINE | ID: mdl-17485245
18.
Statin-associated myopathy with normal creatine kinase levels.
Ann Intern Med
; 137(7): 581-5, 2002 Oct 01.
Article
in English
| MEDLINE | ID: mdl-12353945
19.
Microwave ablation of focal hepatic malignancies regardless of size: A 9-year retrospective study of 64 patients.
Eur J Radiol
; 84(6): 1083-90, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-25818732
20.
The role of methionine in ethylmalonic encephalopathy with petechiae.
Arch Neurol
; 61(4): 570-4, 2004 Apr.
Article
in English
| MEDLINE | ID: mdl-15096407