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Seite 3 für „deficiency“ · Literaturverweise aus öffentlichen Artikeln
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Ascorbic acid deficiency promotes metabolic remodeling and pulmonary fibrosis that leads to respiratory failure in Sod1 and Akr1a double-knockout mice
pubmed · 40616948
Literaturverweis öffnenVitamin B12 deficiency: testing and treatment
pubmed · 42022258
Literaturverweis öffnenDiagnosis and therapy of iron deficiency anemia in pregnancy
pubmed · 3577453
Literaturverweis öffnenAn unusual gastric mass in a patient with human immunodeficiency virus infection
pubmed · 42401513
Literaturverweis öffnenImpact of Estrogen Deficiency on Dry Eye Disease in BRCA Mutation Carriers With Premature Menopause
pubmed · 42241016
Literaturverweis öffnen[Hereditary non-spherocytic hemolytic anemia caused by glucosephosphate isomerase deficiency: 1. case observed in Switzerland].
pubmed · 4419288
Literaturverweis öffnenClinical and Laboratory Profile in Different Types of Primary Immune Deficiency Disorders (PIDs) in Children: A BMU Perspective
doi · 10.21203/rs.3.rs-9964780/v1
Literaturverweis öffnenIntermittent Alternating Eye-Head Synkinesia in GLUT1 Deficiency Syndrome
pubmed · 33607684
Literaturverweis öffnenGonadal function and pathology in 17beta-HSD 3 and 5alpha-reductase deficiency
pubmed · 39782875
Literaturverweis öffnenRiboflavin Deficiency
pubmed · 29262062
Literaturverweis öffnenCopper dysregulation in cardiometabolic disease: copper deficiency versus cuproptosis
pubmed · 42384189
Literaturverweis öffnenProspective Registry of Outcomes, Treatment, and Clinical Trajectories for Anti-IFN-γ Immunodeficiency
pubmed · 42455569
Literaturverweis öffnenA case report of primary central nervous system lymphoma with immune deficiency/disorder setting diagnosed by cerebrospinal fluid cytology
pubmed · 39123330
Literaturverweis öffnenCommon Variable Immune Deficiency and Pregnancy: Improving Outcomes Through Multidisciplinary Care
pubmed · 42194784
Literaturverweis öffnenLate Recognition of Glucose-6-Phosphate Dehydrogenase Deficiency in a 70-Year-Old Man: A Case Report
pubmed · 42245854
Literaturverweis öffnenClinical management and genetic variation analysis of patients with 17β-hydroxysteroid dehydrogenase deficiency
pubmed · 42390145
Literaturverweis öffnenSevere α₁-Antitrypsin Deficiency and Increased Risk of Gastrointestinal Diseases
pubmed · 41885682
Literaturverweis öffnenSevere combined immunodeficiency—an update
pubmed · 26235889
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 öffnenSelenium deficiency-induced cardiomyopathy: a case report
pubmed · 42022031
Literaturverweis öffnenBiotin Deficiency
pubmed · 31613531
Literaturverweis öffnen[Acyl coenzyme A dehydrogenase deficiency of medium-chain fatty acids in a 9-year-old boy with adymia. A rare mitochondrial cytopathy which may be more common than previously assumed].
pubmed · 1775146
Literaturverweis öffnenAcid sphingomyelinase deficiency and Gaucher disease: Underdiagnosed and often treatable causes of hepatomegaly, splenomegaly, and low HDL cholesterol in lean individuals
pubmed · 39774103
Literaturverweis öffnenA case of selective IgG subclass deficiency with STAT3 mutation
pubmed · 27302695
Literaturverweis öffnenAssociation between vitamin D deficiency and adolescent idiopathic scoliosis
pubmed · 42370878
Literaturverweis öffnenA Comprehensive Review of Zinc Deficiency-Associated Anemia
doi · 10.20944/preprints202606.0210.v1
Literaturverweis öffnenBiallelic GTF3A mutations underline a novel human combined immunodeficiency
doi · 10.64898/2026.07.24.26358408
Literaturverweis öffnen[You make the diagnosis. Combined iron and vitamin B 12 deficiency anemia].
pubmed · 6835684
Literaturverweis öffnenApproach to primary immunodeficiency
pubmed · 31690396
Literaturverweis öffnenExpanding the genotypic and phenotypic landscape of ERG Deficiency Syndrome to include aortic/mitral valve insufficiency and aortic aneurysms
doi · 10.21203/rs.3.rs-9719377/v1
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