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Seite 8 für „Deficiency“ · Literaturverweise aus öffentlichen Artikeln
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GATA2 Deficiency Syndrome: A Case Series and Literature Review
pubmed · 41870648
Literaturverweis öffnenExpanding the PKLR mutation spectrum: discovery of two novel variants in two pediatric cases of pyruvate kinase deficiency
pubmed · 42115487
Literaturverweis öffnenThyroid Hormone Deficiency Disrupts Embryonic Ventral Body Wall Development and Myogenesis With Partial Recovery Following LevothyroxineTherapy
pubmed · 40851524
Literaturverweis öffnenCholine Deficiency Drives the Inflammation-Fibrosis Cascade: A Spatiotemporal Atlas of Hepatic Injury from Weeks 6 to 10
pubmed · 41596168
Literaturverweis öffnenAdult-Onset LRBA Deficiency Presenting with Rheumatoid Arthritis-Like Manifestations: A Case Report
pubmed · 42406167
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 öffnenIs acetabular dysplasia and pelvic deformity properly interpreted in patients with congenital femoral deficiency? A 3D analysis of pelvic computed tomography
pubmed · 33204343
Literaturverweis öffnenVitamin D deficiency in Mongolian pregnant women
pubmed · 41956170
Literaturverweis öffnenSynchronous Undifferentiated Embryonal Sarcoma of the Liver and Fibrolamellar Hepatocellular Carcinoma in a Patient with Adenosine Deaminase Deficiency
pubmed · 42283101
Literaturverweis öffnenVitamin K Deficiency Bleeding After Refusal: A Sentinel Event in a Misinformation Era
pubmed · 41916583
Literaturverweis öffnen[Immunologic deficiency syndrome with dysgammaglobulinemia and lymphatic hyperplasia].
pubmed · 4131813
Literaturverweis öffnenFolic acid deficiency as a modifiable risk factor for anastomotic leak in patients undergoing colorectal cancer surgery
pubmed · 40781452
Literaturverweis öffnen17α-hydroxylase deficiency in a 46,XY individual with a hypoplastic uterus: In vitro functional validation of a CYP17A1 mutation
pubmed · 42462819
Literaturverweis öffnenObesity and Its Association With Micronutrient Deficiency Among Mexican Children and Adolescents: A Systematic Review and Meta-analysis
pubmed · 40802583
Literaturverweis öffnenAdulthood diagnosis of Nijmegen breakage syndrome in twins with antibody deficiency clinical presentation
pubmed · 42297123
Literaturverweis öffnenSevere Bone Deformities in Young Children From Vitamin D Deficiency and Fluorosis in Bihar-India
pubmed · 15895280
Literaturverweis öffnenGranulomatous skin lesions of common variable immunodeficiency treated with sirolimus
pubmed · 33660846
Literaturverweis öffnenCongenital vitamin B12 deficiency anemia (Imerslund-Gräsbeck) in 2 HLA identical twins
pubmed · 3600551
Literaturverweis öffnenCase report: co-inheritance of familial lecithin-cholesterol acyltransferase deficiency and α⁰-Thalassemia
pubmed · 42080096
Literaturverweis öffnenSevere congenital factor X deficiency presenting with umbilical and subgaleal hemorrhage: a case report
pubmed · 42144914
Literaturverweis öffnenIncidental pancytopenia in the setting of urolithiasis: severe copper deficiency without classic risk factors
pubmed · 42230009
Literaturverweis öffnenClinical, immunological, treatment characteristics, and outcomes in 22 patients with major histocompatibility complex class II deficiency
pubmed · 42099591
Literaturverweis öffnenVP1 molecular evolution of type 2 immunodeficiency-related vaccine-derived polioviruses (iVDPV2) in a patient with primary immunodeficiency disease (PID)
pubmed · 41629698
Literaturverweis öffnenFIT Testing in Iron Deficiency Anemia: A Retrospective Analysis
pubmed · 41564039
Literaturverweis öffnenManagement and clinical analysis of complications following all-on-4 implant-supported rehabilitation in a patient with severe maxillary bone deficiency and periodontitis: a case report
pubmed · 42304370
Literaturverweis öffnenPrimary Ciliary Dyskinesia: Do We Need to Test for Primary Immune Deficiency Routinely?
pubmed · 41999583
Literaturverweis öffnen[Hereditary or acquired angioedema caused by functional deficiency of C1 inhibitor--a still unfamiliar disease picture].
pubmed · 10093876
Literaturverweis öffnenGoiter prevalence and iodine deficiency disorder among school-age children (6-12 years) in district Ganderbal of Kashmir valley
pubmed · 37546017
Literaturverweis öffnenSevere Combined Immunodeficiency: A Review for Neonatal Clinicians
pubmed · 31261096
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