[Familial incidence of benign recurrent intrahepatic cholestasis]

BM-164 (an H₂S-donor) modulates microRNA expression associated with reperfusion-induced ventricular fibrillation in rat hearts.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences·2026

Window-of-opportunity trials to screen effective agents and optimize dose in breast cancer prevention.

NPJ breast cancer·2025

Curative treatment for oligometastatic gastroesophageal cancer- results of a prospective multicenter study.

Langenbeck's archives of surgery·2024

Oncological outcomes of standard versus prolonged time to surgery after neoadjuvant chemoradiotherapy for oesophageal cancer in the multicentre, randomised, controlled NeoRes II trial.

Annals of oncology : official journal of the European Society for Medical Oncology·2023

Integrated twin-screw wet granulation, continuous vibrational fluid drying and milling: A fully continuous powder to granule line.

International journal of pharmaceutics·2020

Mid-Infrared Imaging Is Able to Characterize and Separate Cancer Cell Lines.

Pathology oncology research : POR·2020

[Structured data collection during neonatal anesthesia: Neo Somno Log - a self-developed digital event tracker].

Orvosi hetilap·2026

[Assessment of dietary habits in adolescents with inflammatory bowel disease].

Orvosi hetilap·2026

[Modern treatment of androgenetic alopecia].

Orvosi hetilap·2026

[A burning challenge in emergency care: burnout, secondary traumatic stress, and psychological immune competence].

Orvosi hetilap·2026

[Triptan treatment in migraine: a dose-based model for persistence and acute medication use patterns using nationwide health insurance data].

Orvosi hetilap·2026

[Patient satisfaction and complications following penile prosthesis implantation].

Orvosi hetilap·2026

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

Pharmacology & therapeutics·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

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[Familial incidence of benign recurrent intrahepatic cholestasis]

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BM-164 (an H₂S-donor) modulates microRNA expression associated with reperfusion-induced ventricular fibrillation in rat hearts.

Window-of-opportunity trials to screen effective agents and optimize dose in breast cancer prevention.

Curative treatment for oligometastatic gastroesophageal cancer- results of a prospective multicenter study.

Oncological outcomes of standard versus prolonged time to surgery after neoadjuvant chemoradiotherapy for oesophageal cancer in the multicentre, randomised, controlled NeoRes II trial.

Integrated twin-screw wet granulation, continuous vibrational fluid drying and milling: A fully continuous powder to granule line.

Mid-Infrared Imaging Is Able to Characterize and Separate Cancer Cell Lines.

[Structured data collection during neonatal anesthesia: Neo Somno Log - a self-developed digital event tracker].

[Assessment of dietary habits in adolescents with inflammatory bowel disease].

[Modern treatment of androgenetic alopecia].

[A burning challenge in emergency care: burnout, secondary traumatic stress, and psychological immune competence].

[Triptan treatment in migraine: a dose-based model for persistence and acute medication use patterns using nationwide health insurance data].

[Patient satisfaction and complications following penile prosthesis implantation].

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

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