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- Clinical picture, diagnosis, treatment and outcome of severe acute respiratory syndrome (SARS) in children
- Neurological post‐acute sequelae of SARS‐CoV‐2 infection
- Ottawa, Ontario, Canada, February 13–16, 2013
- Long-term complications of Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN): the spectrum of chronic problems in patients who survive an episode of SJS/TEN necessitates multidisciplinary follow-up
- Inhalation therapy for repairing damaged elastin fibers and decelerating elastinolysis in chronic obstructive pulmonary disease
- Vitamins
- The pharmacology of methotrexate
- Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
- The Case | Bilateral kidney tumors and lung cysts
- Effects of natural products on skin inflammation caused by abnormal hormones secreted by the adrenal gland
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Case 21-2012
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Phytochemicals as Modulators of Human Endocrine Function: Bridging Traditional Remedies and Hormonal Health
- Pulmonary Hemodynamics in Systemic Hypertension
- Drugs that affect autonomic functions or the extrapyramidal system
- Management of Toxicities of Targeted Therapies
- Relationship between betacoronaviruses and the endocrine system: a new key to understand the COVID-19 pandemic—A comprehensive review
- Cutaneous changes in patients with chronic renal failure on hemodialysis
- Interpretation of Laboratory Data and General Physical Examination by Pharmacists
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Vitamin B-Complex and its Relationship with the Health of Vegetarian People
- Methotrexate in dermatology
- Skin disorders in elderly subjects
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- THE FREQUENCY OF VISCERAL AND PHENOTYPIC MARKERS IN PATIENTS WITH THE COMBINATION OF UNDIFFERENTIATED CONNECTIVE TISSUE DISEASE AND GASTROESOPHAGEAL REFLUX DISEASE
- Cutaneous Markers of Disorders Affecting Adult Horses
- Signal integrator function of CXXC5 in Cancer
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma