• A 5-year-old with connective tissue nevi: Buschke-Ollendorff syndrome
• A case of osteopoikilosis combined with dermal changes and compression syndromes of peripheral nerves
• A female pioneer--doubly recognized
• A novel heterozygous splice-site mutation of LEM domain-containing 3 in a Japanese kindred with Buschke-Ollendorff syndrome
• A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis
• A rare case of secondary syphilis manifesting as immune reconstitution syndrome in an HIV-positive patient
• A twelve-year-old teenager with bone pain and white papules
• Acquired elastoma in a subungual location
• An 8-year-old boy with multiple yellow papules and bony lesions. Buschke-Ollendorff syndrome
• An unusual presentation of Buschke-Ollendorff syndrome
• Buschke-Ollendorf syndrome in a patient with terminal renal failure
• Buschke-Ollendorff syndrome
• Buschke-Ollendorff syndrome
• Buschke-Ollendorff syndrome
• Buschke-Ollendorff syndrome
• Buschke-Ollendorff syndrome
• Buschke-Ollendorff syndrome
• Buschke-Ollendorff syndrome
• Buschke-Ollendorff syndrome
• Buschke-Ollendorff syndrome accidentally diagnosed after a left ankle sprain
• Buschke-Ollendorff syndrome and bilateral cutaneous syndactyly
• Buschke-Ollendorff syndrome associated with elevated elastin production by affected skin fibroblasts in culture
• Buschke-Ollendorff syndrome associated with hypertrophic scar formation: a possible role for LEMD3 mutation
• Buschke-Ollendorff syndrome due to a novel LEMD3 mutation - an unusual case of alopecia
• Buschke-Ollendorff syndrome in a 6-year-old patient: clinical and histopathological aspects of a rare disease
• Buschke-Ollendorff syndrome in a grande multipara: a case report and short review of the literature
• Buschke-Ollendorff syndrome in a three-generation family: influence of a novel LEMD3 mutation to tropoelastin expression
• Buschke-Ollendorff syndrome in two generations imitated Calve-Legg-Perthes disease
• Buschke-Ollendorff syndrome presenting as a painful nodule
• Buschke-Ollendorff syndrome presenting with asymptomatic yellowish papules and leg length discrepancy: A case report
• Buschke-Ollendorff syndrome with LEMD3 germline stopgain mutation p.R678* presenting as multiple subcutaneous nodules with mucin deposition
• Buschke-Ollendorff syndrome with striking phenotypic variation resulting from a novel c.2203C>T nonsense mutation in LEMD3
• Buschke-Ollendorff syndrome with striking phenotypic variation resulting from a novel c.2203C>T nonsense mutation in LEMD3
• Buschke-Ollendorff syndrome--differential diagnosis of disseminated connective tissue lesions
• Buschke-Ollendorff syndrome, otosclerosis, and congenital spinal stenosis
• Buschke-Ollendorff syndrome: a 32-month-old boy with elastomas and craniosynostosis
• Buschke-Ollendorff syndrome: a manifestation of a heterozygous nonsense mutation in the LEMD3 gene
• Buschke-Ollendorff syndrome: a novel case series and systematic review
• Buschke-Ollendorff Syndrome: A Rare Cause of Unilateral Genu Valgum
• Buschke-Ollendorff syndrome: absence of LEMD3 mutation in an affected family
• Buschke-Ollendorff syndrome: early, unilateral and pronounced involvement may be explained as a type 2 segmental manifestation
• Buschke-Ollendorff syndrome: inactivating mutation of the LEMD3 gene
• Buschke-Ollendorff syndrome: report of a case and interpretation of the clinical phenotype as a type 2 segmental manifestation of an autosomal dominant skin disease
• Buschke-Ollendorff syndrome: sparing unnecessary investigations
• Buschke-Ollendorff syndrome: three generations in a Japanese family
• Buschke-Ollendorff syndrome. Connective tissue nevi in osteopoikilosis
• Buschke-Ollendorff-Syndrom mit einer neuartigen LEMD3-Mutation - Der Fall einer ungewöhnlichen Alopezie
• Case report: osteopoikilosis and the Buschke-Ollendorff syndrome
• Connective tissue nevi in children: institutional experience and review
• Connective tissue nevi: an entity revisited
• Deactivating germline mutations in LEMD3 cause osteopoikilosis and Buschke-Ollendorff syndrome, but not sporadic melorheostosis
• Depressed indurated plaque with elastorrhexis as a distinctive lesion in Buschke-Ollendorff syndrome
• Dermatofibrosis lenticularis disseminata with osteopoikilosis. Buschke-Olldendorff syndrome
• Elastic nevus with normal expression of elastin and elastin-related proteins mRNAs
• Elastoma: clinical and histopathological aspects of a rare disease
• 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
• Familial juvenile elastoma
• Familial localized connective tissue nevus of the scalp with alopecia (report of a very unusual case)
• Familial syndromes with skin tumor markers
• Family Buschke-Ollendorff syndrome
• Germline LEMD3 mutations are rare in sporadic patients with isolated melorheostosis
• Helen Ollendorff Curth: A dermatologist's lasting legacy
• Helen Ollendorff-Curth: A dermatologist's lasting legacy
• Identification of a Novel Point Mutation in the LEMD3 Gene in an Infant With Buschke-Ollendorff Syndrome
• Juvenile elastoma without germline mutations in LEMD3 gene: A case of Buschke-Ollendorff syndrome?
• Juvenile elastoma: a forme fruste of the Buschke-Ollendorff syndrome?
• LEM domain-containing protein 3 antagonizes TGFβ-SMAD2/3 signaling in a stiffness-dependent manner in both the nucleus and cytosol
• Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis
• MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-beta signaling
• Melorheostosis and Osteopoikilosis Clinical and Molecular Description of an Italian Case Series
• Melorheostosis: a Rare Sclerosing Bone Dysplasia
• Melorheostosis: A Review of the Literature and a Case Report
• 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
• Morphometric analysis of elastic skin fibres from patients with: cutis laxa, anetoderma, pseudoxanthoma elasticum, and Buschke-Ollendorff and Williams-Beuren syndromes
• Novel and recurrent germline LEMD3 mutations causing Buschke-Ollendorff syndrome and osteopoikilosis but not isolated melorheostosis
• Novel Somatic Mutation in LEMD3 Splice Site Results in Buschke-Ollendorff Syndrome with Polyostotic Melorheostosis and Osteopoikilosis
• Ossifying fibroma in Buschke-Ollendorff syndrome
• Osteopoikilosis and multiple exostoses caused by novel mutations in LEMD3 and EXT1 genes respectively--coincidence within one family
• Osteopoikilosis: a case report
• Osteopoikilosis: report of a familial case
• Osteopokilosis
• Papular elastorrhexis and Buschke-Ollendorff syndrome are different entities
• Papular elastorrhexis, a distinctive entity?
• Papular elastorrhexis: a distinct variant of connective tissue nevi or an incomplete form of Buschke-Ollendorff syndrome?
• Papular elastorrhexis: a variant of dermatofibrosis lenticularis disseminata (Buschke-Ollendorff syndrome)?
• Papular elastorrhexis: clinical perspectives
• Papular elastorrhexis. report of five cases
• Regulation of elastin synthesis in pathological states
• RNA recognition motif of LEMD3 as a key player in the pathogenesis of Buschke-Ollendorff syndrome
• Segmental type 2 manifestation of autosome dominant skin diseases. Development of a new formal genetic concept
• Spotted bones in an osteopoikilosis-related disease (Buschke Ollendorff Syndrome): Identifying this rare condition from the lab to the field
• Structural basis for receptor-regulated SMAD recognition by MAN1
• The 12q14 microdeletion syndrome: additional patients and further evidence that HMGA2 is an important genetic determinant for human height
• The Buschke-Ollendorff syndrome presenting as familial elastic tissue naevi
• The Buschke-Ollendorff syndrome: a case report of simultaneous osteo-cutaneous malformations in the hand
• The heterozygous Lemd3 +/GT mouse is not a murine model for osteopoikilosis in humans
• Two cases of papular elastorrhexis
• Variable expressivity in Buschke-Ollendorff syndrome
• What syndrome is this? Buschke-Ollendorff syndrome