Buschke-Ollendorff Syndrome Latest Advances

Clinical and Histopathological Characteristics of Buschke-Ollendorff Syndrome: A Case Series.

Journal: Acta dermato-venereologica

Published: November 18, 2024

Eponyms that honor Jewish dermatologists: A celebration and a remembrance, Part two: Jewish physicians who practiced between 1933 and 1945.

Journal: Clinics in dermatology

Published: September 30, 2023

Buschke-Ollendorff Syndrome: A Rare Cause of Unilateral Genu Valgum.

Journal: Cureus

Published: April 24, 2023

Melorheostosis: A Review of the Literature and a Case Report.

Journal: Medicina (Kaunas, Lithuania)

Published: February 24, 2023

Buschke-Ollendorff syndrome presenting with asymptomatic yellowish papules and leg length discrepancy: A case report.

Journal: Journal of musculoskeletal & neuronal interactions

Published: June 01, 2022

Variable expressivity in Buschke-Ollendorff syndrome.

Journal: Annales de dermatologie et de venereologie

Published: February 18, 2021

Spotted bones in an osteopoikilosis-related disease (Buschke Ollendorff Syndrome): Identifying this rare condition from the lab to the field.

Journal: International journal of paleopathology

Published: November 29, 2020

Buschke-Ollendorff syndrome in a 6-year-old patient: clinical and histopathological aspects of a rare disease.

Journal: Acta dermatovenerologica Alpina, Pannonica, et Adriatica

Published: March 25, 2020

Buschke-Ollendorff syndrome with LEMD3 germline stopgain mutation p.R678* presenting as multiple subcutaneous nodules with mucin deposition.

Journal: Journal of cutaneous pathology

Published: March 07, 2020

Modeling-based bone formation transforms trabeculae to cortical bone in the sclerotic areas in Buschke-Ollendorff syndrome. A case study of two females with LEMD3 variants.

Journal: Bone

Published: February 06, 2020

Depressed indurated plaque with elastorrhexis as a distinctive lesion in Buschke-Ollendorff syndrome.

Journal: Pediatric dermatology

Published: January 17, 2020

Melorheostosis and Osteopoikilosis Clinical and Molecular Description of an Italian Case Series.

Journal: Calcified tissue international

Published: March 18, 2019

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Clinical and Histopathological Characteristics of Buschke-Ollendorff Syndrome: A Case Series.

Clinical and Histopathological Characteristics of Buschke-Ollendorff Syndrome: A Case Series.

Eponyms that honor Jewish dermatologists: A celebration and a remembrance, Part two: Jewish physicians who practiced between 1933 and 1945.

Eponyms that honor Jewish dermatologists: A celebration and a remembrance, Part two: Jewish physicians who practiced between 1933 and 1945.

Buschke-Ollendorff Syndrome: A Rare Cause of Unilateral Genu Valgum.

Buschke-Ollendorff Syndrome: A Rare Cause of Unilateral Genu Valgum.

Melorheostosis: A Review of the Literature and a Case Report.

Melorheostosis: A Review of the Literature and a Case Report.

Buschke-Ollendorff syndrome presenting with asymptomatic yellowish papules and leg length discrepancy: A case report.

Buschke-Ollendorff syndrome presenting with asymptomatic yellowish papules and leg length discrepancy: A case report.

Variable expressivity in Buschke-Ollendorff syndrome.

Variable expressivity in Buschke-Ollendorff syndrome.

Spotted bones in an osteopoikilosis-related disease (Buschke Ollendorff Syndrome): Identifying this rare condition from the lab to the field.

Spotted bones in an osteopoikilosis-related disease (Buschke Ollendorff Syndrome): Identifying this rare condition from the lab to the field.

Buschke-Ollendorff syndrome in a 6-year-old patient: clinical and histopathological aspects of a rare disease.

Buschke-Ollendorff syndrome in a 6-year-old patient: clinical and histopathological aspects of a rare disease.

Buschke-Ollendorff syndrome with LEMD3 germline stopgain mutation p.R678* presenting as multiple subcutaneous nodules with mucin deposition.

Buschke-Ollendorff syndrome with LEMD3 germline stopgain mutation p.R678* presenting as multiple subcutaneous nodules with mucin deposition.

Modeling-based bone formation transforms trabeculae to cortical bone in the sclerotic areas in Buschke-Ollendorff syndrome. A case study of two females with LEMD3 variants.

Modeling-based bone formation transforms trabeculae to cortical bone in the sclerotic areas in Buschke-Ollendorff syndrome. A case study of two females with LEMD3 variants.

Depressed indurated plaque with elastorrhexis as a distinctive lesion in Buschke-Ollendorff syndrome.

Depressed indurated plaque with elastorrhexis as a distinctive lesion in Buschke-Ollendorff syndrome.

Melorheostosis and Osteopoikilosis Clinical and Molecular Description of an Italian Case Series.

Melorheostosis and Osteopoikilosis Clinical and Molecular Description of an Italian Case Series.