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「"Marjanović D "[Author]」の検索結果

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Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.

Genetic variation study on fifteen STR loci in isolated Slovenian "Inland Island" human populations of the Selška Valley Region.

A Candidate Gene Association Study of FKBP5 and CRHR1 Polymorphisms in Relation to War-Related Posttraumatic Stress Disorder.

The Role of TaqI DRD2 (rs1800497) and DRD4 VNTR Polymorphisms in Posttraumatic Stress Disorder (PTSD).

Role of the Allelic Variation in the 5-Hydroxytryptamine Receptor 1A (HTR1A) and the Tryptophan Hydroxylase 2 (TPH2) Genes in the Development of PTSD.

Association of Neuropeptide S Receptor 1 and Glutamate Decarboxylase 1 Gene Polymorphisms with Posttraumatic Stress Disorder.

The Association of Catechol-O-Methyl-Transferase and Interleukin 6 Gene Polymorphisms with Posttraumatic Stress Disorder.

Associations between Polymorphisms in the Solute Carrier Family 6 Member 3 and the Myelin Basic Protein Gene and Posttraumatic Stress Disorder.

Associations of Gene Variations in Neuropeptide Y and Brain Derived Neurotrophic Factor Genes with Posttraumatic Stress Disorder.

Genetic Susceptibility to Posttraumatic Stress Disorder: Analyses of the Oxytocin Receptor, Retinoic Acid Receptor-Related Orphan Receptor A and Cannabinoid Receptor 1 Genes.

Association Analysis of Maoa and Slc6a4 Gene Variation in South East European War Related Posttraumatic Stress Disorder.

Population study of thrombophilic markers and pharmacogenetic markers of warfarin prevalence in Bosnia and Herzegovina.

Y chromosome genetic data defined by 23 short tandem repeats in a Serbian population on the Balkan Peninsula.

Phylogeny of Paleozoic limbed vertebrates reassessed through revision and expansion of the largest published relevant data matrix.

Association Between - 675 ID, 4G/5G PAI-1 Gene Polymorphism and Pregnancy Loss: A Systematic Review.

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.

Pharmacogenetics of novel oral anticoagulants: a review of identified gene variants & future perspectives.

The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant.

Monoamine oxidase A gene methylation and its role in Posttraumatic Stress Disorder - First evidence from the South Eastern Europe (SEE)-PTSD study.

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