• A case of Mulibrey nanism with associated Wilms' tumor
• A diverse family of proteins containing tumor necrosis factor receptor-associated factor domains
• A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy
• A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity
• A proteomic study of the downregulation of TRIM37 on chondrocytes: Implications for the MULIBREY syndrome
• A stone was lifted from her heart: pericardial constriction in 28-year-old patient with Mulibrey nanism
• Antibody deficiency and isolated growth hormone deficiency in a girl with Mulibrey nanism
• Ascites and nuchal fold as the first signs of progressive cardiac diastolic dysfunction in a fetus with fetal growth restriction due to mulibrey nanism
• Ascites in Mulibrey syndrome
• Assessment of mulibrey nanism cardiopathy with functional magnetic resonance imaging
• Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis
• Cardiac dysfunction in children with mulibrey nanism
• Cardiac involvement in Mulibrey nanism: characterization with magnetic resonance imaging
• CD4(+) T Cell Defects in a Mulibrey Patient With Specific TRIM37 Mutations
• CD4⁺ T Cell Defects in a Mulibrey Patient With Specific <em>TRIM37</em> Mutations
• Characterisation of the mulibrey nanism-associated TRIM37 gene: transcription initiation, promoter region and alternative splicing
• Constrictive Pericarditis and Primary Amenorrhea with Syndactyly in an Iranian Female: Mulibrey Nanism Syndrome
• Constrictive pericarditis with dwarfism in two siblings (mulibrey nanism)
• Craniofacial and dental study of mulibrey nanism
• Expression of MUL, a gene encoding a novel RBCC family ring-finger protein, in human and mouse embryogenesis
• Failure of sexual maturation in Mulibrey nanism
• Familial intrauterine nanism with constrictive pericarditis, the MuLiBrEy syndrome
• Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism
• Growth and growth hormone therapy in subjects with mulibrey nanism
• Growth failure with pericardial constriction. The syndrome of mulibrey nanism
• Gynecological tumors in Mulibrey nanism and role for RING finger protein TRIM37 in the pathogenesis of ovarian fibrothecomas
• High frequency of tumours in Mulibrey nanism
• High-resolution physical and genetic mapping of the critical region for Meckel syndrome and Mulibrey Nanism on chromosome 17q22-q23
• Insulin resistance syndrome in subjects with mutated RING finger protein TRIM37
• Is autosomal recessive Silver-Russel syndrome a separate entity or is it part of the 3-M syndrome spectrum?
• Letter: Mulibrey nanism v. hereditary congenital dwarfism with pericardial constriction
• Liver pathology and biochemistry in patients with mutations in TRIM37 gene (Mulibrey nanism)
• Mass ascites in Mulibrey nanism
• MULIBREY (MUscle, LIver, BRain, EYe) nanism. Report of a new case
• Mulibrey heart disease: clinical manifestations, long-term course, and results of pericardiectomy in a series of 49 patients born before 1985
• Mulibrey nanism
• Mulibrey nanism and immunological complications: a comprehensive case report and literature review
• Mulibrey Nanism and the Real Time Use of Genome and Biobank Engines to Inform Clinical Care in an Ultrarare Disease
• Mulibrey nanism and Wilms tumor
• Mulibrey nanism in a 35 year-old Iranian female with constrictive pericarditis
• Mulibrey nanism in a Mexican child
• Mulibrey Nanism Syndrome: A Case for Heart Transplantation
• Mulibrey nanism--a novel peroxisomal disorder
• Mulibrey nanism, an autosomal recessive syndrome with ocular involvement
• Mulibrey nanism, an autosomal recessive syndrome with pericardial constriction
• Mulibrey nanism; an inherited dysmorphic syndrome with characteristic ocular findings
• Mulibrey nanism: clinical features and diagnostic criteria
• Mulibrey nanism: review of 23 cases of a new autosomal recessive syndrome
• Mulibrey nanism: three additional patients and a review of 39 patients
• Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing
• Mulibrey syndrome: anesthetic management
• Mulibrey-nanism: dwarfism with muscle, liver, brain and eye involvement
• Neuraxial anesthesia in a parturient with Leri-Weill dyschondrosteosis
• New intragenic rearrangements in non-Finnish mulibrey nanism
• Novel mutations in the TRIM37 gene in Mulibrey Nanism
• Pericardial Constriction and Myocardial Restriction in Pediatric Mulibrey Nanism: A Complex Disease With Diastolic Dysfunction
• Peroxisomal functions in mulibrey nanism
• Premature ovarian insufficiency and early depletion of the ovarian reserve in the monogenic Mulibrey nanism disorder
• Refractory congestive heart failure following delayed pericardectomy in a 12-year-old child with Mulibrey nanism due to a novel mutation in TRIM37
• Renal findings in patients with Mulibrey nanism
• Report of two Syrian siblings with Mulibrey nanism
• Restriction of lung volumes but normal function of pulmonary tissue in mulibrey nanism
• Segmental cystic kidney tumours in children
• Serum levels of natriuretic peptides in children with various types of loading conditions
• So-called mulibrey nanism with pericardial constriction
• Successful Total Pericardiectomy for Constrictive Pericarditis in the First Series of Japanese Patients With Mulibrey Nanism
• Syndrome Mulibrey Nanism. A case report and autopsy findings in a 8-month-old girl (author's transl)
• Targeted Next Generation Sequencing Approach in Patients Referred for Silver-Russell Syndrome Testing Increases the Mutation Detection Rate and Provides Decisive Information for Clinical Management
• Testicular failure and male infertility in the monogenic Mulibrey nanism disorder
• The cardiopathy of mulibrey nanism, a new inherited syndrome
• The Importance of Early Pericardiectomy in Mulibrey Nanism Syndrome, a Case Report
• The TRIM37 gene encodes a peroxisomal RING-B-box-coiled-coil protein: classification of mulibrey nanism as a new peroxisomal disorder
• The TRIM37 variants in Mulibrey nanism patients paralyze follicular helper T cell differentiation
• Thoracoscopic pericardiectomy for constrictive pericarditis in a pediatric patient with mulibrey nanism
• Tissue expression of the mulibrey nanism-associated Trim37 protein in embryonic and adult mouse tissues
• TRIM37 defective in mulibrey nanism is a novel RING finger ubiquitin E3 ligase
• TRIM37 deficiency induces autophagy through deregulating the MTORC1-TFEB axis
• TRIM37 is highly expressed during mitosis in CHON-002 chondrocytes cell line and is regulated by miR-223
• TRIM37 prevents formation of centriolar protein assemblies by regulating Centrobin
• TRIM37 prevents formation of condensate-organized ectopic spindle poles to ensure mitotic fidelity
• Trim37-deficient mice recapitulate several features of the multi-organ disorder Mulibrey nanism
• TRIM37, a novel E3 ligase for PEX5-mediated peroxisomal matrix protein import
• TRIM37: a critical orchestrator of centrosome function
• TRIMming down to TRIM37: Relevance to Inflammation, Cardiovascular Disorders, and Cancer in MULIBREY Nanism
• Two B or not two B? Overview of the rapidly expanding B-box family of proteins
• Variants in 46,XY DSD-Related Genes in Syndromic and Non-Syndromic Small for Gestational Age Children with Hypospadias
• Where genetics and pathology meet: mulibrey nanism
• Whole Exome Sequencing Identified the Causative Mutation in a 4-Year-Old Female with Mulibrey Nanism: A Case Report
• Wilms tumor with Mulibrey Nanism: A case report and review of literature
• Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism