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Sounira Mehri is an expert in Neurology at University of Monastir (Tunisia). Sounira Mehri has authored 150 publications, the most recent in 2026. SLR score: 536 (community average: 125). How the SLR is computed.

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Sounira Mehri University of Monastir Tunisia
536 ScienceLeadR Reputation 536

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Neurology

Subspecialties: Cardiology - Critical Care - Biochemistry

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Expert Rankings

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Organizations

Career arc: 2010 - 2026
Source: PubMed

University of Monastir

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 150

Citations

Citations: 534 1st author: 55 Last author: 71 Unique author: 0

Main journals

Neurosciences (Riyadh) 7
Eur J Neurol 4
J Renin Angiotensin Aldosterone Syst 4
Malays Fam Physician 4
Archives of Cardiovascular Diseases Supplements 3

Best Journals

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Rule Out Myelitis Prior to Cutting Into a Child's Back Because of Progressive Tetraparesis.
PMID 42800723 — emergency medicine, myelitis, spinal cord injuries, syringomyelia		J Emerg Med20260
Based on a Single Case, Cardiopulmonary Training Cannot Be Recommended as Therapy for Hemiparesis in MELAS With Ischemic Stroke.
PMID 42757572 — ischemic stroke, stroke, melas syndrome, therapeutics		Kaohsiung J Med Sci20260
The diagnosis of diabetic striatopathy should be made only after careful exclusion of all possible differential diagnoses.
PMID 42757271 — diagnosis, differential, diagnosis		Malays Fam Physician20260
The quality of death certificates depends on the training, competence and independence of the issuers, and the intensity of the investigation into the cause of death.
PMID 42626813 — quality control, cause of death, public health, education, death certificates, autopsy		East Mediterr Health J20260
CK-MM screening using neonatal dried blood spots may be inadequate at detecting all dystrophin mutation carriers.
PMID 42591777 — blood, dystrophin, mutation		Transl Pediatr20260

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Sources: PubMed, OpenAlex, ClinicalTrials, EU CTIS