MEFV sequence variants and amyloidosis: still an enigmatic question

Identifying cancer in the French National Health Data System (SNDS): an updated scoping review of algorithms, validation and applications.

Journal of epidemiology and population health·2026

Evolution of characteristics and outcomes for patients hospitalized for COVID-19 during successive waves of the epidemic in France.

Annals of epidemiology·2026

Defects in meiosis I contribute to the genesis of androgenetic hydatidiform moles.

The Journal of clinical investigation·2024

The significance of carrying MEFV variants in symptomatic and asymptomatic individuals.

Clinical genetics·2024

Functional diversity of NLRP3 gain-of-function mutants associated with CAPS autoinflammation.

The Journal of experimental medicine·2024

[Autoinflammatory diseases in children: The contribution of genetics].

La Revue du praticien·2024

Mutation Severity of FBXO43 Determines Spermatogenic Outcome and Informs Precision ART Strategies.

Human mutation·2026

Mitochondrial tRNASer(AGY) 12234A > G Mutation May Contribute to the Clinical Expression of Hypertrophic Cardiomyopathy-Associated tRNAIle 4263A > G Mutation.

Human mutation·2026

Splice effect of a synonymous variant in AP4B1: multiomics approach establishes the diagnosis in two sisters with spastic paraplegia.

Human mutation·2026

Integrated Mutation Profiling and Prognostic Genomic Signature in Pediatric Testicular and Ovarian Germ Cell Tumors.

Human mutation·2026

Molecular Characterization of TSC1 and TSC2 Variants in a Greek Cohort of Tuberous Sclerosis Complex Patients.

Human mutation·2026

Structural Genomics Defines PBRM1 Bromodomain Variant Function in ccRCC.

Human mutation·2026

Quality of Service and Cost of Managing an Episode of Major Depressive Disorder: A Cohort Study in Iran.

Archives of Iranian medicine·2026

Assessment of Susceptibility of Methicillin-Resistant Staphylococcus aureus Isolates to Ceftaroline and Other Antistaphylococcal Agents.

Cureus·2026

Progressive Human Orf Virus Infection in a Kidney Transplant Recipient Successfully Treated with Cryotherapy Without Modification of Immunosuppression: A Case Report.

International journal of nephrology and renovascular disease·2026

The impact of minimally invasive mitral valve surgery on early postoperative organ dysfunction.

JTCVS open·2026

Circulating miRNAs for glioblastoma monitoring: from biofluid to clinical decision.

Molecular therapy. Oncology·2026

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MEFV sequence variants and amyloidosis: still an enigmatic question

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Identifying cancer in the French National Health Data System (SNDS): an updated scoping review of algorithms, validation and applications.

Evolution of characteristics and outcomes for patients hospitalized for COVID-19 during successive waves of the epidemic in France.

Defects in meiosis I contribute to the genesis of androgenetic hydatidiform moles.

The significance of carrying MEFV variants in symptomatic and asymptomatic individuals.

Functional diversity of NLRP3 gain-of-function mutants associated with CAPS autoinflammation.

[Autoinflammatory diseases in children: The contribution of genetics].

Mutation Severity of FBXO43 Determines Spermatogenic Outcome and Informs Precision ART Strategies.

Mitochondrial tRNASer(AGY) 12234A > G Mutation May Contribute to the Clinical Expression of Hypertrophic Cardiomyopathy-Associated tRNAIle 4263A > G Mutation.

Splice effect of a synonymous variant in AP4B1: multiomics approach establishes the diagnosis in two sisters with spastic paraplegia.

Integrated Mutation Profiling and Prognostic Genomic Signature in Pediatric Testicular and Ovarian Germ Cell Tumors.

Molecular Characterization of TSC1 and TSC2 Variants in a Greek Cohort of Tuberous Sclerosis Complex Patients.

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Assessment of Susceptibility of Methicillin-Resistant Staphylococcus aureus Isolates to Ceftaroline and Other Antistaphylococcal Agents.

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MEFV sequence variants and amyloidosis: still an enigmatic question

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