• A case of Madelung's disease accompanied by Klinefelter's syndrome
• A case report on Madelung's disease and comprehensive review of the literature
• A middle-aged man with increasing body fat
• Analysis of pelvic lipomatosis and a case report of two brothers
• Benign symmetrical Launois-Bensaude type II lipomatosis with market systemic involvement and psoriasis
• Benign symmetrical lipomatosis with predominant localization in the neck area (Madelung's disease)
• Beyond cervical lipomas: myoclonus, gait disorder and multisystem involvement leading to mitochondrial disease
• Calcyphosine-like (CAPSL) is regulated in Multiple Symmetric Lipomatosis and is involved in Adipogenesis
• Central nervous system involvement in multiple symmetric lipomatosis
• Coexistence of dyschondrosteosis associated to <em>SHOX</em> deficiency, pseudohypoparathyroidism 1B, and chronic autoimmune thyroiditis: a case report
• Cutaneous lipomatosis: diagnosing a rare condition
• Cytophagic histiocytic panniculitis with haemophagocytosis in a patient with familial multiple lipomatosis and review of the literature
• Do you know this syndrome?
• Dysarthria, progressive parkinsonian features and symmetric necrosis of putamen in a family with painful lipomas (Dercum disease variant)
• Epidural angiolipoma and multiple familial lipomatosis
• Eruptive familial angiolipomas occurring during pregnancy
• Familial multiple (asymmetrical) lipomatosis associated with small intestinal leiomyoma
• Familial multiple angiolipomatosis
• Familial multiple lipomatosis
• Familial multiple lipomatosis: a case report
• Familial multiple lipomatosis. Report of a case and a review of the literature
• Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNA
• Familial multiple symmetric lipomatosis with peripheral neuropathy
• Homozygous Familial Hypercholesterolemia Associated with Symmetric Subcutaneous Lipomatosis
• Homozygous LIPE mutation in siblings with multiple symmetric lipomatosis, partial lipodystrophy, and myopathy
• Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathy
• How to diagnose a lipodystrophy syndrome
• Imaging spectrum of abnormal subcutaneous and visceral fat distribution
• Insulin sensitivity and metabolic clearance rate of insulin in familial multiple lipomatosis
• Insulin sensitivity in Familial Multiple Lipomatosis
• LIPE-related lipodystrophic syndrome: clinical features and disease modeling using adipose stem cells
• Lipolysis of lipomas in patients with familial multiple lipomatosis: an ultrasonography-controlled trial
• Lipomatoses
• Lipomatosis, proximal myopathy, and the mitochondrial 8344 mutation. A lipid storage myopathy?
• Lipomatous disorder of the peri-trochanteric soft tissue: case report and review
• Madelung-like deformity in pseudohypoparathyroidism type 1b
• Madelung's disease mimicking deep vein thrombosis: an unusual case
• Madelung's disease: a case report
• Madelung's disease: comorbidities, fatty mass distribution, and response to treatment of 22 patients
• MFN2-associated lipomatosis: Clinical spectrum and impact on adipose tissue
• Mitochondrial DNA rearrangements in young onset parkinsonism: two case reports
• Multiple familial angiolipomatosis: treatment of liposuction
• Multiple familial lipomatosis with polyneuropathy, an inherited dominant condition
• Multiple lipomas linked to an RB1 gene mutation in a large pedigree with low penetrance retinoblastoma
• Multiple lipomatosis in a patient with familial atypical mole syndrome
• Multiple spindle cell lipomas: a report of 7 familial and 11 nonfamilial cases
• Multiple symmetric and multiple familial lipomatosis
• Multiple symmetric lipomatosis
• Multiple Symmetric Lipomatosis (Madelung Disease) in a Large Canadian Family With the Mitochondrial <em>MTTK</em> c.8344A&gt;G Variant
• Multiple Symmetric Lipomatosis (Madelung Disease) in a Large Canadian Family With the Mitochondrial MTTK c.8344A>G Variant
• Multiple symmetrical lipomatosis with familial polineuropathy
• Non-symmetric subcutaneous lipomatosis associated with familial combined hyperlipidaemia
• Rare adipose disorders (RADs) masquerading as obesity
• Review of Dercum's disease and proposal of diagnostic criteria, diagnostic methods, classification and management
• Roch's lipomatosis in univitelline twin sisters
• Sporadic multiple lipomatosis: a case report and review of the literature
• Subcutaneous Adipose Tissue Diseases: Dercum Disease, Lipedema, Familial Multiple Lipomatosis, and Madelung Disease
• Subcutaneous adipose tissue fatty acid desaturation in adults with and without rare adipose disorders
• Subcutaneous Nodules in a Kidney Transplant Recipient: Familial Multiple Lipomatosis
• Symmetric lipomatoses in female patients
• Syndromic lipomatosis of the head and neck: a review of the literature
• Testicular seminoma in a patient with familial multiple (asymmetrical) lipomatosis
• The nasopalpebral lipoma-coloboma syndrome: a new autosomal dominant dysplasia-malformation syndrome with congenital nasopalpebral lipomas, eyelid colobomas, telecanthus, and maxillary hypoplasia
• Unusual distribution of the lower body fatty tissue: classification, treatment, and differential diagnosis