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Seite 3 für „Hereditary“ · Literaturverweise aus öffentlichen Artikeln
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[Hereditary and acquired toxoplasmosis of the eye].
pubmed · 13039311
Literaturverweis öffnenHereditary neuroendocrine gastroenteropancreatic tumors and multiple endocrine neoplasia type 1
pubmed · 15011133
Literaturverweis öffnenCase 10: A patient with an isolated prolongation of the activated partial thromboplastin time without a bleeding problem – severe hereditary Factor XII deficiency
pubmed · 10517121
Literaturverweis öffnenHereditary methemoglobinemia diagnosed in adulthood: Type 1 cytochrome B5 reductase deficiency
pubmed · 42319687
Literaturverweis öffnenThe Complex Clinical and Genetic Landscape of Hereditary Peripheral Neuropathy
pubmed · 33497257
Literaturverweis öffnenHereditary Spherocytosis: A Case Series Spanning Prenatal Detection to Neonatal Care
pubmed · 42175794
Literaturverweis öffnenImpaired hepatic metabolism in Hereditary Fructose Intolerance confers fructose-independent risk for steatosis and hypertriglyceridemia
pubmed · 41423081
Literaturverweis öffnenHereditary Lymphedema of the Leg - A Case Report
pubmed · 28785330
Literaturverweis öffnenHuman intestinal disaccharidases and hereditary disaccharide intolerance. The hydrolysis of sucrose, isomaltose, palatinose (isomaltulose), and a 1,6-alpha-oligosaccharide (isomalto-oligosaccharide) preparation
pubmed · 14024642
Literaturverweis öffnenMolecular Basis of Hereditary Persistence of Fetal Hemoglobin
pubmed · 9668525
Literaturverweis öffnenPrevalence and Incidence of Hereditary Angioedema: A Systematic Literature Review
pubmed · 42485266
Literaturverweis öffnenHereditary Hemolytic Anemia Due to PIEZO1 Red Blood Cell Membrane Defect
pubmed · 39593245
Literaturverweis öffnenLoss-of-function of EBP50 is a new cause of hereditary peripheral neuropathy: EBP50 functions in peripheral nerve system
pubmed · 32077526
Literaturverweis öffnenHereditary disorders of ineffective erythropoiesis
pubmed · 39938185
Literaturverweis öffnenCharacterization of hereditary angioedema population in Argentina: A nationwide study
pubmed · 42292763
Literaturverweis öffnenSpecificity of the human intestinal disaccharidases and implications for hereditary disaccharide intolerance
pubmed · 13883118
Literaturverweis öffnenIncreasing evidence of hereditary lymphedema caused by CELSR1 loss-of-function variants
pubmed · 31215153
Literaturverweis öffnenThree cases of hereditary hypomagnesemia with secondary hypocalcemia caused by novel TRPM6 gene mutations and a literature review
pubmed · 42324811
Literaturverweis öffnen[Molecular biology analysis: hereditary hemochromatosis, Wilson disease, alpha 1-antitrypsin deficiency and Dubin-Johnson syndrome].
pubmed · 9824945
Literaturverweis öffnenFrom Splenectomy to Partial Splenic Embolization, Which is Better for Hereditary Spherocytosis?
pubmed · 42039086
Literaturverweis öffnenCurrent Status of Molecular Diagnosis of Hereditary Hemolytic Anemia in Korea
pubmed · 38742293
Literaturverweis öffnenEndometrial Cancer. Guideline of the DGGG, DKG and DKH (S3-Level, AWMF Registry Number 032/034-OL, September 2022). Part 1 with Recommendations on the Epidemiology, Screening, Diagnosis and Hereditary Factors of Endometrial Cancer, Geriatric Assessment and Supply Structures
pubmed · 37588260
Literaturverweis öffnenFROM DISCOVERY SCIENCE TO THE CLINIC - HERITABLE ENDOCRINE CANCERS AND RELATED DISORDERS: Functional imaging in hereditary endocrine neoplasms: evolving modalities and clinical implications
pubmed · 42274298
Literaturverweis öffnenDiagnostic yield of targeted next-generation sequencing for pediatric hereditary hemolytic anemia
pubmed · 37697358
Literaturverweis öffnenSpectrum of Hereditary Neuropathies in Adult Patients From Serbia
pubmed · 42476530
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