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Seite 25 für „Gene“ · Literaturverweise aus öffentlichen Artikeln
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ANCA-associated vasculitis: From immunopathogenesis to diagnosis and toward precision therapy
pubmed · 42480954
Literaturverweis öffnenUterus unicornis mit rudimentärem Horn und ipsilateraler Nierenagenesie:Klinische Symptomatik und Therapie
pubmed · 7657144
Literaturverweis öffnen[The malignant degeneration of congenitally misplaced testicles].
pubmed · 24307
Literaturverweis öffnenPrenatal Imaging of Micrognathia, Micromelia, and Fetal Hydrops Leading to the Diagnosis of Achondrogenesis Type II with a COL2A1 Missense Mutation
pubmed · 41373627
Literaturverweis öffnenInitial Tendon Retraction is Associated with Muscle Degeneration After Nonoperatively Treated Proximal Hamstring Avulsions
pubmed · 42089934
Literaturverweis öffnenMpox (formerly monkeypox): pathogenesis, prevention and treatment
pubmed · 38148355
Literaturverweis öffnenImmunopathogenesis and immunoregulatory mechanisms in allergic contact dermatitis
pubmed · 42212145
Literaturverweis öffnenNeonatal Diabetes Mellitus Due to Homozygous ZNF808 Mutation Associated With Skeletal Anomalies: A Novel Presentation of Pancreatic Agenesis-3
pubmed · 41809312
Literaturverweis öffnenUrinary Bladder Agenesis in a Child: An Uncommon Congenital Anomaly of the Urinary Tract
pubmed · 40263187
Literaturverweis öffnenEnhancing ascitic fungal infection diagnosis through next-generation sequencing: a pilot study in surgical ICU patients
pubmed · 39554813
Literaturverweis öffnenThe distinct effects of metabolic syndrome on negative symptoms and on antipsychotic therapy of schizophrenia involve insular volume, functional connectivity, and genetic polymorphisms
pubmed · 42386701
Literaturverweis öffnenPathogenesis, Diagnosis, and Clinical Management of Aortic Aneurysms: Current Status and Future Perspectives
pubmed · 42416586
Literaturverweis öffnenCiclosporin-Induced Generalised Hypertrichosis in a Transgender Woman Receiving Testosterone Blockers
pubmed · 41822646
Literaturverweis öffnenGenetics of Hb F/F Cell Variance in Adults and Heterocellular Hereditary Persistence of Fetal Hemoglobin
pubmed · 9859924
Literaturverweis öffnenClinical and prognostic implications of pituitary tumor-transforming gene 1 in solid tumors
pubmed · 42434759
Literaturverweis öffnenClinical heterogeneity in congenital factor XII deficiency: Coexisting risk factors in thrombotic and bleeding events
pubmed · 42381238
Literaturverweis öffnen[Genetic distribution in Chinese patients with hereditary peripheral neuropathy]
pubmed · 36241230
Literaturverweis öffnenCorrection to: Gastrointestinal juvenile-like (inflammatory/hyperplastic) mucosal polyps in neurofibromatosis type 1 with no concurrent genetic or clinical evidence of other syndromes
pubmed · 30306267
Literaturverweis öffnenAge-related macular degeneration: a socioeconomic time bomb in our aging society
pubmed · 16924447
Literaturverweis öffnenLungenembolie
pubmed · 26621816
Literaturverweis öffnenHas the introduction of increased genetic prenatal testing affected rates of termination of pregnancy due to fetal abnormality?
pubmed · 38348952
Literaturverweis öffnenA bladder cancer-associated gene signature for exploratory qPCR-based survival stratification in NAC-Treated muscle-invasive bladder cancer
pubmed · 42482080
Literaturverweis öffnenHBV PreS/S gene mutations in patients with chronic hepatitis B
pubmed · 42498832
Literaturverweis öffnenMucopolysaccharidosis type II in tunisian families: IDS gene variations disrupting substrate binding and a novel deep intronic deletion reducing IDS expression
pubmed · 42489956
Literaturverweis öffnen[The gonadal dysgenesis syndrome].
pubmed · 5650506
Literaturverweis öffnenHereditary sideroblastic anemia: pathophysiology and gene mutations
pubmed · 20848343
Literaturverweis öffnenDie chronische intestinale Pseudoobstruktion: Pathogenese, Diagnostik und Therapie
pubmed · 11857104
Literaturverweis öffnenDental Erosion Management: From Remineralization to Emerging Regenerative Approaches-A Narrative Review
pubmed · 41744553
Literaturverweis öffnenThe Pathogenesis of Lupus Nephritis
pubmed · 23929771
Literaturverweis öffnenReport of a Homozygous Nonsense Variant in the WDR91 Gene Associated With Severe Communicating Hydrocephalus, Dandy Walker Malformation, and Cerebellar Hypoplasia
pubmed · 42311177
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