Gezielt nachschlagen
Suche
Suche startet nach einer kurzen Eingabepause.
Hier finden Sie Quellen, die öffentliche HealthOS-Artikel zitieren. Im lokalen PubMed-Bestand recherchieren → · In der Fallbibliothek suchen →
28 angezeigte Treffer · Seite 1, keine Gesamtzahl für „familial“ · Literaturverweise aus öffentlichen Artikeln
Suchtreffer
Quellen in Artikeln
Prenatal, Perinatal, and Familial Risk Factors in the Differential Diagnosis Between Autism Spectrum Disorder and Phenylketonuria: A Retrospective Case-Control Study in the Absence of Neonatal Screening
pubmed · 42496180
Literaturverweis öffnenFear of cancer recurrence across sporadic, familial and hereditary breast cancer: the role of genetic risk and psychosocial factors
doi · 10.21203/rs.3.rs-9306007/v1
Literaturverweis öffnenEffects of evolocumab on plasma coenzyme Q10 in patients with heterozygous familial hypercholesterolemia
pubmed · 42389346
Literaturverweis öffnenGenetic analysis of three familial cases of pure terminal 19p13.3 duplication caused by maternal balanced translocation t(19;21) (p13.3;p12)
pubmed · 42306095
Literaturverweis öffnenDetection of a Distinct Erythropoietin (EPO) Profile After Isoelectric Focusing in Patients With Familial Erythrocytosis
pubmed · 41713879
Literaturverweis öffnenA Hematologic Masquerader: Progressive Familial Intrahepatic Cholestasis Type 3 Presenting as Anemia, Hepatosplenomegaly, and Recurrent Bleeding in a Child
pubmed · 42328328
Literaturverweis öffnen[Homozygote familial hypercholesterinemia. Pathophysiology and genetic control of cholesterol metabolism].
pubmed · 207958
Literaturverweis öffnenProneness to infections and familial risk of tic disorders
pubmed · 42015626
Literaturverweis öffnenFamilial complex regional pain syndrome in pediatric siblings: a diagnostic challenge and therapeutic success-a case report
pubmed · 41937140
Literaturverweis öffnenEULAR/PReS endorsed recommendations for the management of familial Mediterranean fever (FMF): 2024 update
pubmed · 40234174
Literaturverweis öffnenPancreatitis in Familial Dysautonomia Patients
pubmed · 42348501
Literaturverweis öffnen[Myoglobinuria and familial hematuria with dominant autosomal transmission: mitochondrial disorder or basal lamina disorder?].
pubmed · 8966475
Literaturverweis öffnen"Familial Is Not Always Genetic: Two Brothers with Dystonia and Oculomotor Apraxia Secondary to Rh Incompatibility-Induced Kernicterus"
pubmed · 42340156
Literaturverweis öffnenEGLN1-positive familial erythrocytosis: a rare variant with an unusually aggressive clinical course
pubmed · 40627222
Literaturverweis öffnenThe Genetics of Familial Neoplastic Thyroid Disease and Primary Hyperparathyroidism
pubmed · 42419309
Literaturverweis öffnenFamilial predisposition to flap necrosis after palatoplasty: a case report of two siblings with bilateral cleft palate
pubmed · 40898970
Literaturverweis öffnenNewborn Screening for Familial Hypercholesterolemia Using Liquid Chromatography Tandem Mass Spectrometry-Based Free Cholesterol Measurements
pubmed · 42229728
Literaturverweis öffnenPCSK9 rs562556 variant and survival in BRCA1 mutation carriers and mutation-negative familial breast cancer
pubmed · 42297814
Literaturverweis öffnenFamilial Chylomicronemia Syndrome: A Clinical Guide for Endocrinologists
pubmed · 30183397
Literaturverweis öffnenA Comparative Study Between Flax Seeds and Psyllium Husk as a 6-month Adjuvant Nutraceutical in Pediatric Patients with Familial Hypercholesterolemia
doi · 10.21203/rs.3.rs-9695072/v1
Literaturverweis öffnenAn overview of genetic predisposition to familial hematological malignancies
pubmed · 34052033
Literaturverweis öffnenKcnq2 R213 knock-in mice reveal variant- and region-specific mechanisms underlying self-limited familial neonatal-infantile epilepsy and early infantile developmental and epileptic encephalopathy
pubmed · 41742307
Literaturverweis öffnenPeripheral neuron phenotypes of familial dysautonomia are rescued by AAV-mediated gene therapy
pubmed · 41957238
Literaturverweis öffnenFatal familial insomnia and Agrypnia Excitata: Autonomic dysfunctions and pathophysiological implications
pubmed · 30890351
Literaturverweis öffnenCase report: co-inheritance of familial lecithin-cholesterol acyltransferase deficiency and α⁰-Thalassemia
pubmed · 42080096
Literaturverweis öffnenThe Unfolding of Familial CARD14- Associated Papulosquamous Eruption (CAPE) and a Brief Review
pubmed · 41762009
Literaturverweis öffnenRecognizing Familial Thyroid Neoplasia: The Pathologist's Role in Diagnosis and Management
pubmed · 42319956
Literaturverweis öffnenTen-year clinical course of familial lecithin-cholesterol acyltransferase deficiency caused by Cys74Tyr mutation leading to dialysis and multiple systemic complications: a case report
pubmed · 42159827
Literaturverweis öffnen