• A 17-year-old adolescent with anorexia and gait abnormalities: Camurati-Engelmann syndrome
• A case of papilledema in Camurati-Engelmann disease treated effectively with prednisolone
• A Case Report of a 44-Year-Old Woman With Camurati-Englemann Disease: A Case Report
• A common presentation of a rare genetic disorder clinically mimicking primary myopathy
• A family with Camurati-Engelman disease: the role of the missense p.R218C mutation in TGFbeta1 in bones and endocrine glands
• A family with Camurati-Engelman disease. The role of the missense p.R218C mutation in TGFB1 in bones and endocrine glands
• A new case of Melnick-Needles syndrome with skeletal manifestations: A case report
• A new LRP6 variant and Camurati-Engelmann-like disease
• A patient with Camurati-Engelmann disease presenting bilateral TMJ ankylosis: A case report
• A Rare Sporadic Case of Camurati-Engelmann Disease With Jaw Involvement
• Aberrant activation of latent transforming growth factor-β initiates the onset of temporomandibular joint osteoarthritis
• Aberrant activation of TGF-beta1 induces high bone turnover via Rho GTPases-mediated cytoskeletal remodeling in Camurati-Engelmann disease
• Aberrant activation of TGF-β1 induces high bone turnover <em>via</em> Rho GTPases-mediated cytoskeletal remodeling in Camurati-Engelmann disease
• Alteration of Bone Density, Microarchitecture, and Strength in Patients with Camurati-Engelmann Disease: Assessed by HR-pQCT
• An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes
• Anesthesia for a child with Camurati-Engelmann disease
• Angioid streaks in a case of Camurati-Engelmann disease
• Anterior Total Hip Arthroplasty With Bulk Femoral Head Autograft in a Patient With Camurati-Engelmann Disease
• Bilateral papilloedema in Camurati-Engelmann disease
• Bone-targeted delivery of TGF-beta type 1 receptor inhibitor rescues uncoupled bone remodeling in Camurati-Engelmann disease
• Bone-targeted delivery of TGF-β type 1 receptor inhibitor rescues uncoupled bone remodeling in Camurati-Engelmann disease
• Camurati-Engelmann disease
• Camurati-Engelmann disease
• Camurati-Engelmann Disease
• Camurati-Engelmann disease (progressive diaphyseal dysplasia): reports of an Indian kindred
• Camurati-engelmann disease association with hypogonadism and primary hypothyroidism
• Camurati-Engelmann disease combined with transethmoidal meningoencephalocele: illustrative case
• Camurati-Engelmann Disease Complicated by Hypopituitarism: Management Challenges and Literature Review of Outcomes With Bisphosphonates
• Camurati-Engelmann disease in a family from Croatian Island: an old bone scan confirmed pattern of inheritance
• Camurati-Engelmann disease or Ribbing disease
• Camurati-Engelmann Disease with Good Treatment Response to Losartan
• Camurati-Engelmann disease with obesity in a newly identified family carrying a missense p.Arg156Cys mutation in the TGFB1 gene
• Camurati-Engelmann disease--a rare cause of bone pain
• Camurati-Engelmann disease-a rare cause of tetany identified on bone scintigraphy: A case report
• Camurati-Engelmann disease: a case report
• Camurati-Engelmann disease: a case report from sub-Saharan Africa
• Camurati-Engelmann Disease: A Case-Based Review About an Ultrarare Bone Dysplasia
• Camurati-Engelmann disease: New clinical insights in an Egyptian case report
• Clinical characteristics and identification of a novel TGFB1 variant in three unrelated Chinese families with Camurati-Engelmann disease
• Clinical characteristics and the influence of rs1800470 in patients with Camurati-Engelmann disease
• Clinical characteristics and treatment outcomes in Camurati-Engelmann disease: A case series
• Clinical diagnosis and mutation analysis of a Chinese family with Camurati-Engelmann disease
• Correlative bone imaging in a case of Schnitzler's syndrome and brief review of the literature
• Decompression of the internal auditory canal via the retrosigmoid approach in a patient with Camurati-Engelmann disease: illustrative case
• Diagnosing Camurati-Engelmann disease-the age of whole-exome sequencing
• Discrepancy between bone density and bone material strength index in three siblings with Camurati-Engelmann disease
• Dual Biologic Therapy in an Adolescent With Camurati-Engelmann Disease and Crohn Disease
• Efficacy of denosumab therapy after alendronate treatment for a 66-year-old woman with Camurati-Engelmann disease and osteoporosis: a case report
• Elimination of pain and improvement of exercise capacity in Camurati-Engelmann disease with losartan
• Excess TGF-β mediates muscle weakness associated with bone metastases in mice
• Failure of conventional treatment and losartan in Camurati-Engelmann disease: A case report
• Genetic testing is useful in adults with limited phenotypes of genetic skeletal conditions
• Heterozygous mutations in the straitjacket region of the latency-associated peptide domain of TGFB2 cause Camurati-Engelmann disease type II
• Hyperactive transforming growth factor-β1 signaling potentiates skeletal defects in a neurofibromatosis type 1 mouse model
• Hypothalamic amenorrhea in a Camurati-Engelmann disease--a case report
• Imaging aspects of Camurati-Engelmann disease
• Imaging features and differential diagnosis of multiple diaphyseal sclerosis: A case report and review of literature
• Improvement of Bone Health and Initiation of Puberty Development in Camurati-Engelmann Disease With Glucocorticoid and Losartan Treatment: A Case Report and Review of Literature
• Intramedullary reaming in Ribbing disease
• Localization of the gene for hyperostosis cranialis interna to chromosome 8p21 with analysis of three candidate genes
• Looking for new anabolic treatment from rare diseases of bone formation
• Looking for the skeleton in the closet-rare genetic diagnoses in patients with diabetes and skeletal manifestations
• Losartan as a Steroid-Sparing Adjunct in a Patient With Features of Refractory Camurati-Engelmann Disease
• Meniere-like syndrome in Camurati-Engelmann disease
• Mild Camurati-Engelamann disease presenting with exophthalmos as the first and only manifestation: A case report
• Mild Camurati‑Engelamann disease presenting with exophthalmos as the first and only manifestation: A case report
• Miscellaneous Bone Disorders
• Multiple diaphyseal sclerosis (Ribbing disease): what about neridronate?
• Observations on the Natural History of Camurati-Engelmann Disease
• Orthopedic Manifestations of Type I Camurati-Engelmann Disease
• Osteosclerotic disease and bone cyst in a prehispanic burial from Las Canadas del Teide (Tenerife, Canary Islands)
• Pain improvement in Camurati-Engelmann disease after anti-TNFalpha therapy
• Pain improvement in Camurati-Engelmann disease after anti-TNFα therapy
• Papilledema Treated by Cranial Expansion in a 5-Year-Old Boy with Camurati-Engelmann Syndrome
• Positive effects of an angiotensin II type 1 receptor antagonist in Camurati-Engelmann disease: a single case observation
• Proband and the Brother
• Progressive diaphyseal dysplasia: a rare bone disorder with alarming radiographs
• Reduced Dentin Matrix Protein Expression in Camurati-Engelmann Disease Transgenic Mouse Model
• Regarding Camurati-Engelmann Disease: In Reply
• Regarding Camurati-Engelmann Disease: To the Editor
• Repeat Intracranial Expansion After Skull Regrowth in Hyperostotic Disease: Technical Note
• Reply to: Whole-Body Magnetic Resonance Imaging in Camurati-Engelmann Disease
• Ribbing disease of tibia: a rare entity
• Ribbing disease: a systematic review
• Ribbing disease: apropos of a case
• Seropositive Rheumatoid Arthritis with Very Unusual X-ray Findings
• Significant Improvement After Surgery for a Symptomatic Osteoblastoma in a Patient with Camurati-Engelmann Disease: Case Report and Literature Review
• Significant Improvement of Clinical Symptoms, Bone Lesions, and Bone Turnover after Long-Term Zoledronic Acid Treatment in Patients with a Severe Form of Camurati-Engelmann Disease
• Skeletal Dysplasia Presenting as a Neuromuscular Disorder - Report of a Family with Camurati-Engelmann Syndrome
• Surgery Treatment of an Adult Patient with Camurati-Engelmann Disease: A Case Report
• The Impact of Genetic Variability of TGF-Beta Signaling Biomarkers in Major Craniofacial Syndromes
• Total Hip Arthroplasty in a Patient with Camurati-Engelmann Disease: A Case Report
• Transforming growth factor-beta1 gene mutations and phenotypes in pediatric patients with Camurati-Engelmann disease
• Transforming growth factor-β1 gene mutations and phenotypes in pediatric patients with Camurati‑Engelmann disease
• Treatment of Ribbing disease with 5-year follow-up and literature review
• Treatment responses in five patients with Ribbing disease including two with 466C&gt;T missense mutations in TGFβ1
• Treatment responses in five patients with Ribbing disease including two with 466C>T missense mutations in TGFbeta1
• Vecuronium was safely used in a patient with Engelmann's disease without muscle weakness
• Visual and otologic manifestation of Camurati-Engelmann's disease: a case report
• Whole-Body Magnetic Resonance Imaging in Camurati-Engelmann Disease