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Research 361–390 of 1000+
- The IVIG treatment response in autoimmune polyendocrine syndromes type 2 with anti-GAD65 antibody-associated stiff person syndrome: a case report and literature review
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Cronkhite-Canada syndrome: A case report and literature review
- EFFECT OF THYROID DYSFUNCTION ON BODY MASS INDEX AND HORMONAL IMBALANCE IN WOMEN HAVING POLYCYSTIC OVARIAN SYNDROME
- Schimmelpenning Syndrome: A Neuro-Oculo-Cutaneous Disorder
- Bachmann–Bupp syndrome and treatment
- [Commentary] The Polyfollicular Anovulatory Androgenic Syndrome: A New Label for an Old Syndrome
- Autoimmune Polyglandular Syndrome Type 3-D
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Neuroendokrine paraneoplastische Syndrome
- Autoimmune polyglandular syndrome type 4 – case report
- Hair Loss in Children
- Potential PRP Hair Treatment Side Effects
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Crystalline Cataract and Uncombable Hair
- Menkes Syndrome Presenting as Myoclonic Seizures: Neuroimaging and EEG Observations
- Light Microscopic Hair Abnormalities in Children: Retrospective Review of 119 Cases in a 10-Year Period
- Acquired Uncombable Hair
- Clinical, Microscopic and Ultrastructural Findings in a Case of Short Anagen Syndrome
- Recurrent bacterial vaginosis and Netherton's syndrome
- Deimination in epidermal barrier and hair formation
- Hair That Is Difficult to Manage in a Hispanic Girl
- Hair loss in infancy and childhood
- What is ‘normal’ hair?
- Low-dose oral minoxidil in a case of short anagen syndrome
- 1440 DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control keratinocyte differentiation and hair growth
- Loose anagen syndrome in one identical twin girl.
- 712 Using scanning electron microscopy to elucidate the role of hair shaft malformation in the pathogenesis of Central Centrifugal Cicatricial Alopecia