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Items: 1 to 20 of 1103

1.

The mitochondrial calcium uniporter: a new therapeutic target for Parkinson's disease-related cardiac dysfunctions?

Scorza FA, Menezes-Rodrigues FS, Olszewer E, Errante PR, Tavares JGP, Scorza CA, Ferraz HB, Finsterer J, Caricati-Neto A.

Clinics (Sao Paulo). 2020 Jan 10;75:e1299. doi: 10.6061/clinics/2020/e1299. eCollection 2020. No abstract available.

2.

Myasthenic crises triggering Takotsubo cardiomyopathy.

Scorza FA, Fiorini AC, Scorza CA, Finsterer J.

Int J Cardiol. 2020 Feb 1;300:48. doi: 10.1016/j.ijcard.2019.11.084. No abstract available.

PMID:
31928654
3.

Muscle biopsy is not diagnostic for MELAS.

Finsterer J.

J Neurol Sci. 2020 Jan 3;410:116670. doi: 10.1016/j.jns.2020.116670. [Epub ahead of print] No abstract available.

PMID:
31923614
4.

Fentanyl can be mitochondrion -toxic depending on dosage and cell type.

Finsterer J, Zarrouk-Mahjoub S.

J Anaesthesiol Clin Pharmacol. 2019 Oct-Dec;35(4):570-571. doi: 10.4103/joacp.JOACP_262_18. No abstract available.

5.

Letter to the Editor: POLG1 variants may secondarily affect mtDNA load and structure.

Finsterer J.

Rom J Morphol Embryol. 2019;60(3):1073-1074. No abstract available.

6.

Side effects of and contraindications for whole-body electro-myo-stimulation: a viewpoint.

Stöllberger C, Finsterer J.

BMJ Open Sport Exerc Med. 2019 Dec 17;5(1):e000619. doi: 10.1136/bmjsem-2019-000619. eCollection 2019. Review.

7.

Heart failure and late leaks should be considered as late complications of left atrial appendage occlusion.

Stöllberger C, Finsterer J, Schneider B.

Europace. 2020 Jan 6. pii: euz356. doi: 10.1093/europace/euz356. [Epub ahead of print] No abstract available.

PMID:
31904852
8.

Disturbed regional right heart mechanics assessed by strain echocardiography in genetically diverse hypoplastic left heart syndrome.

Finsterer J, Scorza FA.

Int J Cardiol. 2020 Jan 1;298:74-75. doi: 10.1016/j.ijcard.2019.08.020. No abstract available.

PMID:
31901266
9.

Overlapping Phenotype from Double Trouble SMARCA2 and POLG1 Variants c.2556A > C and c.3708G > T, Respectively.

Finsterer J.

Neuropediatrics. 2019 Dec 30. doi: 10.1055/s-0039-3402008. [Epub ahead of print] No abstract available.

PMID:
31887771
10.

Cerebrospinal-fluid ATP is inappropriate as a biomarker of disease severity and treatment response in MELAS.

Finsterer J.

Mitochondrion. 2019 Dec 24. pii: S1567-7249(19)30322-8. doi: 10.1016/j.mito.2019.12.006. [Epub ahead of print] No abstract available.

PMID:
31881280
11.

Low Heteroplasmy Rates Argue Against the m.3243A>G Variant as the Cause of Auditory Agnosia.

Finsterer J.

Neurologist. 2020 Jan;25(1):10. doi: 10.1097/NRL.0000000000000247. No abstract available.

PMID:
31876652
12.

The Spectrum of Neuromuscular Disorders Admitted to a Pediatric Intensive Care Unit Is Broader Than Anticipated.

Finsterer J.

J Child Neurol. 2019 Dec 23:883073819894852. doi: 10.1177/0883073819894852. [Epub ahead of print] No abstract available.

PMID:
31868086
13.

Heteroplasmy Rates of the m.14495A>G variant in MT-ND6 May Not Predict the Phenotype of LHON.

Finsterer J, Aliyev R.

Transl Vis Sci Technol. 2019 Dec 18;8(6):42. doi: 10.1167/tvst.8.6.42. eCollection 2019 Nov. No abstract available.

14.
15.

Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion.

Finsterer J.

Mov Disord. 2019 Dec;34(12):1931-1932. doi: 10.1002/mds.27905. No abstract available.

PMID:
31845759
16.

Low heteroplasmy rates in clinically affected m.3243A > G carriers not necessarily explain the phenotype.

Finsterer J.

J Neurol Sci. 2019 Dec 5;409:116614. doi: 10.1016/j.jns.2019.116614. [Epub ahead of print] No abstract available.

PMID:
31835213
17.

MELAS in a Walk-in Customer.

Finsterer J.

J Neurosci Rural Pract. 2019 Oct;10(4):725-727. doi: 10.1055/s-0039-1700618. Epub 2019 Dec 11. No abstract available.

18.

Pathogenicity of the variant m.13376 T > C in ND5 remains unproven.

Finsterer J.

J Neurol Sci. 2019 Dec 5;409:116615. doi: 10.1016/j.jns.2019.116615. [Epub ahead of print] No abstract available.

PMID:
31830610
19.

Viability of diffusion tensor imaging for assessing retro-chiasmatic involvement in Kearns-Sayre syndrome remains elusive.

Finsterer J.

Neuroradiology. 2020 Feb;62(2):131-132. doi: 10.1007/s00234-019-02325-7. Epub 2019 Dec 6. No abstract available.

PMID:
31807840
20.

Congenital nystagmus, disability, visual impairment, and noncompaction suggest hereditary disease.

Finsterer J.

Einstein (Sao Paulo). 2019 Dec 2;17(4):eCE5251. doi: 10.31744/einstein_journal/2019CE5251. English, Portuguese. No abstract available.

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