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25 angezeigte Treffer · Seite 3, keine Gesamtzahl für „some“ · Literaturverweise aus öffentlichen Artikeln
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Active Clinical Trials in Hepatic Encephalopathy: Something Old, Something New and Something Borrowed
pubmed · 36977964
Literaturverweis öffnen[Ergotism of the locomotor apparatus--a sometimes forgotten diagnosis?].
pubmed · 1557579
Literaturverweis öffnenPlasma and Sonophoresis-Assisted Topical Delivery of an Exosome for Androgenic Alopecia
pubmed · 41945329
Literaturverweis öffnenPrenatal diagnosis of congenital diaphragmatic hernia with mosaicism of chromosomes 17q and 18q in Iran: a case report
pubmed · 42082986
Literaturverweis öffnenPreliminary Clinical Outcomes of Human Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes in Chronic Rhinosinusitis With Nasal Polyps: A Case Report
pubmed · 42117288
Literaturverweis öffnenSome Religious and Spiritual Experiences Associated with Depression Resemble Hypomania/Mania
doi · 10.31234/osf.io/ew5mh_v1
Literaturverweis öffnenInfluence of X-Chromosome Inactivation in Pathogenesis of Turner Syndrome
pubmed · 42496531
Literaturverweis öffnenThe Extra X Chromosome and Autoimmune Susceptibility in Klinefelter Syndrome
pubmed · 42400286
Literaturverweis öffnenCurrent survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies
pubmed · 32449585
Literaturverweis öffnenThe epidemiology of sex chromosome abnormalities
pubmed · 32506765
Literaturverweis öffnenTrace Element Deficiency in Systemic Sclerosis-Too Much Effort for Some Traces?
pubmed · 38999801
Literaturverweis öffnenChild Neurology: Triosephosphate isomerase deficiency
pubmed · 32873690
Literaturverweis öffnenM2 macrophage-derived exosomes improves secondary lymphedema through cellular mitochondrial homeostasis regulation via the Keap1-Nrf2/mPTP axis
pubmed · 42500645
Literaturverweis öffnenCase Report: Rare triple-line chromosome 9 mosaicism (47,XX,+del(9)(q13)/47,XX,+9/46,XX) associated with severe neurodevelopmental impairment and congenital anomalies
pubmed · 42017141
Literaturverweis öffnen[The personality of the poliomyelitis patient with bladder disorders, with some remarks on the management of the sequelae of poliomyelitis].
pubmed · 13321868
Literaturverweis öffnenWhy Some Patients Choose Nutritional Therapy over Medications and Surgery in Obesity Care
pubmed · 41901125
Literaturverweis öffnenExposome involvement in the development of acne vulgaris
pubmed · 41924258
Literaturverweis öffnenA review of the roles of exosomes in salivary gland diseases with an emphasis on primary Sjögren's syndrome
pubmed · 39873057
Literaturverweis öffnenPrenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result
pubmed · 34247824
Literaturverweis öffnenComputational Modelling of Platysma Muscle Mechanics: Challenging the Isometric Contraction Paradigm and Implications for the Treatment of Neck Bands
pubmed · 42377494
Literaturverweis öffnenClinical and Biological Insights into Myelodysplastic Neoplasms Associated with Deletions of Chromosome 5q Region
pubmed · 41440765
Literaturverweis öffnenGastric volvulus associated with preduodenal portal vein in right isomerism: a case report
pubmed · 42338707
Literaturverweis öffnenThe Role of Inflammasome in the Pathogenesis of Alopecia Areata: NLRP3 and Its Cascade Contribute to the Onset and Early Stage of Alopecia Areata
pubmed · 42244274
Literaturverweis öffnenMacular and optic nerve hypoplasia in chromosome 2p partial trisomy
pubmed · 41290552
Literaturverweis öffnenTaraxacum officinale-derived exosome-like nanovesicles modulate gut metabolites to prevent intermittent hypoxia-induced hypertension
pubmed · 36963360
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