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    Research 571–600 of 1000+

    1. Hair-Thread Tourniquet Syndrome; Emergent Diagnosable Condition Archives of pediatric surgery · 2022
    2. Treatment of widespread alopecia areata in young patients with monthly oral corticosteroid pulse. Pediatric Dermatology · 1998 · 48 citations
    3. Treatment of Widespread Alopecia Areata in Young Patients with Monthly Oral Corticosteroid Pulse Pediatric Dermatology · 1998 · 18 citations
    4. Pustular Eruption in a Patient Treated With Trametinib Pediatric Dermatology · 2025
    5. Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene Clinical Pediatric Endocrinology · 1992 · 3 citations
    6. Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa Pediatric dermatology · 2023
    7. Iatrogenic Cushing's Syndrome in a Patient With Salt-Wasting Congenital Adrenal Hyperplasia (SWCAH) Journal of pediatric nursing · 2011
    8. 869 AN EVALUATION OF ZINC STATUS IN PATIENTS WITH ANOREXIA NERVOSA Pediatric research · 1978
    9. Concomitant Vitiligo and Psoriasis in a Patient Treated with Interferon Alfa‐2a for Chronic Hepatitis B Infection Pediatric Dermatology · 2004 · 60 citations
    10. Cushing's syndrome due to pharmacological interaction in a cystic fibrosis patient Acta pædiatrica · 2002 · 6 citations
    11. Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function <i>VDR</i> mutation 2018 · 6 citations
    12. Abnormalities in the hair morphology of patients with some but not all types of mucopolysaccharidoses European journal of pediatrics · 2007 · 22 citations
    13. Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant Pediatrics International · 2026
    14. Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes 2017 · 4 citations
    15. Linear Alopecia Areata in a 4-year-old Patient: A Rare Clinical Variant Indian Journal of Paediatric Dermatology · 2025
    16. Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations Hormone research in paediatrics · 2010 · 62 citations
    17. Cushing's syndrome due to pharmacological interaction in a cystic fibrosis patient Acta pædiatrica · 2002 · 37 citations
    18. Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome Journal of pediatric & adolescent gynecology · 2019 · 1 citations
    19. Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets International Journal of Contemporary Pediatrics · 2023
    20. Epidemiology, clinical features, and outcome of the hospitalized patients with Kerion in Fars Province, Iran: an eleven-year retrospective study BMC Pediatrics · 2024 · 1 citations
    21. Association of early-onset androgenetic alopecia with metabolic syndrome: A case–control study on 46 patients in a tertiary care hospital in South India Indian Journal of Paediatric Dermatology · 2018
    22. Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation 2019 · 1 citations
    23. Vitamin D-dependent rickets type II: extreme end organ resistance to 1,25-dihydroxy vitamin D3 in a patient without alopecia European journal of pediatrics · 1986 · 50 citations
    24. Netherton Syndrome Associated with Growth Hormone Deficiency Pediatric Dermatology · 2013 · 21 citations
    25. To Treat or Not to Treat: Two Roads Traveled With Alopecia Areata Pediatric Dermatology · 2025
    26. A New Case of Trichothiodystrophy Associated with Autism, Seizures, and Mental Retardation Pediatric Dermatology · 1997 · 10 citations
    27. Case 2-2022: An Adolescent Male in Cardiac Arrest 3 Days After Liver Transplantation for End-Stage Liver Disease Pediatric Critical Care Medicine · 2022 · 3 citations
    28. Rapid full engraftment and successful immune reconstitution after allogeneic hematopoietic stem cell transplantation with reduced intensity conditioning in Omenn syndrome Pediatric transplantation · 2009 · 8 citations
    29. Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome European Journal of Pediatrics · 2013 · 15 citations
    30. Answer International Journal of Pediatrics and Adolescent Medicine · 2015 · 1 citations