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Seite 17 für „congenita“ · Literaturverweise aus öffentlichen Artikeln
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Comparison of nuclear renographic renal cortical transit time with diuretic drainage time parameters in congenital hydronephrosis
pubmed · 41722508
Literaturverweis öffnenCongenital Tricuspid Valve Stenosis with Small Ostium Secundum Atrial Septal Defect and Ventricular Septal Defect Eisenmenger Complex
pubmed · 40028245
Literaturverweis öffnenClean intermittent catheterization reverses hydronephrosis in a child with congenital nephrogenic diabetes insipidus: a case report
pubmed · 42415594
Literaturverweis öffnenCongenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation
pubmed · 12933587
Literaturverweis öffnenVertical transmission of scrub typhus: a case report of congenital infection
pubmed · 40734243
Literaturverweis öffnenTrans-anastomotic tube feeding following repair of congenital duodenal obstruction: A 15-year single-centre cohort study
pubmed · 42250629
Literaturverweis öffnen22q11.2 deletion syndrome and congenital heart disease
pubmed · 32049433
Literaturverweis öffnenCongenital Bilateral Complete Agenesis of the Hallucal Sesamoids: A Case Report
pubmed · 42152882
Literaturverweis öffnenReview of Congenital Myasthenic Syndrome Caused by Pathogenic Variants in GFPT1
pubmed · 42387671
Literaturverweis öffnenCongenital malformations of the female genital organs
pubmed · 38334344
Literaturverweis öffnenCase Report: Blepharophimosis and Ptosis as Leading Dysmorphic Features of Rare Congenital Malformation Syndrome With Developmental Delay - New Cases With TRAF7 Variants
pubmed · 34513876
Literaturverweis öffnenCurrarino syndrome: a comprehensive genetic review of a rare congenital disorder
pubmed · 33836786
Literaturverweis öffnenCongenital Thrombocytosis, Hepatosplenomegaly, and Rash in a Term Neonate
pubmed · 42344867
Literaturverweis öffnenCongenital Hypoglossia With Craniofacial Anomalies Without Limb Defects: A Rare Phenotypic Variant of Oromandibular-Limb Hypogenesis Syndrome
pubmed · 42440826
Literaturverweis öffnenImplications of segmental and lobar tracheobronchial anomalies in congenital heart disease: a 12-year retrospective CT analysis
pubmed · 41858563
Literaturverweis öffnenNeonatal cyanosis: exploring the complexity of coexisting congenital methemoglobinaemia and pulmonary hypertension
pubmed · 42156105
Literaturverweis öffnenMultiplex targeted high-throughput sequencing in a series of 352 patients with congenital limb malformations
pubmed · 31502745
Literaturverweis öffnenCongenital Anomalies of the Knee-Hypoplasia of the Meniscus: A Case Report
pubmed · 42158592
Literaturverweis öffnenCongenital Alopecia, Hypoplastic Kidneys, Growth Restriction, Growth Hormone Resistance, and Liver Fibrosis: Confirmation of a New Syndrome Caused by Biallelic Variants in ZPR1
pubmed · 40776660
Literaturverweis öffnenCharacteristics and environmental susceptibility of first-pass meconium microbiota in neonates with congenital intestinal atresia
pubmed · 42442462
Literaturverweis öffnenNotes from the Field: Congenital Rubella Syndrome - Florida, 2025
pubmed · 41785150
Literaturverweis öffnenCongenital rectal stenosis diagnosed using an anoscope to detect a mucosal web with an orifice: a case report
pubmed · 41768332
Literaturverweis öffnenA diagnostic pitfall: Advanced labyrinthitis ossificans simulating congenital inner ear malformation on CT and MRI
pubmed · 41158321
Literaturverweis öffnen[Congenital scoliosis].
pubmed · 2660068
Literaturverweis öffnenTranscatheter Advances in the Treatment of Adult and Congenital Valvular Heart Disease
pubmed · 26407545
Literaturverweis öffnenResection and double pericardial patch repair of a congenital aneurysm of the mitral-aortic intervalvular fibrosa
pubmed · 37578351
Literaturverweis öffnenA comparison of the severity of tricuspid valve regurgitation between echocardiographic and cardiac magnetic resonance criteria in adults with congenital heart disease
pubmed · 42257018
Literaturverweis öffnenDisrupted Vestibular Nuclei Neuron Development in a Chick Model for Congenital Vestibular Disorders
pubmed · 42281183
Literaturverweis öffnen[The echographic diagnosis of a rare congenital uterine anomaly (uterus unicornis with a rudimentary noncommunicating horn)].
pubmed · 9471906
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