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Research 91–120 of 115
- Ischemic Vaso-occlusive Retinopathy as Initial Presentation in Pediatric Systemic Lupus Erythematosus: A Case Report
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- TONGUE, RED
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- ROBERTSONIAN TRANSLOCATION PATIENT WITH RECURRENT MISCARRIAGE
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- Disseminated Small Papules on the Face: A Quiz
- Dissociated Human Dermal Papilla Cells Induce Hair Follicle Neogenesis in Grafted Dermal–Epidermal Composites
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Isolation and Characterization of a Fetal-Maternal Microchimeric Stem Cell Population in Maternal Hair Follicles Long after Parturition
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Autoamputation in a 45-Year-Old Female with Systemic Lupus Erythematosus Overlap with Systemic Sclerosis: A Case Report
- Abstracts from the 17th Congress of the European Society for Dermatology and Psychiatry
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- Anti-DFS70 sebagai Penanda Kejadian Autoimun Nonsistemik (Primary Billiar Cholangitis) pada Systemic Lupus Erythematosus
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review
- Interstitial pneumonia with autoimmune features: challenges and controversies
- A Rare Case of Cutis Verticis Gyrata with Underlying Cerebriform Intradermal Nevus
- Asociación entre disfunción eréctil y funcionalidad del subsistema conyugal en pacientes con hiperplasia prostática benigna
- Hair Disorders in Autoimmune Diseases
- 1329 CENPV is a novel CYLD-interacting molecule regulating ciliary acetylated tubulin
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Physiologic functions of PP2A: Lessons from genetically modified mice
- Two-ligand priming mechanism for potentiated phosphoinositide synthesis is an evolutionarily conserved feature of Sec14-like phosphatidylinositol and phosphatidylcholine exchange proteins