• A novel de novo PDGFRB variant in a child with severe cerebral malformations, intracerebral calcifications, and infantile myofibromatosis
• A Rare Case of Infantile Myofibromatosis Presenting to the Emergency Department as Undiagnosed Long Bone Fractures
• A Rare Case of Infantile Myofibromatosis With Intra Cranial Involvement
• A Recurrent Cheek Mass
• A SAMD5-SASH1 fusion in solitary infantile myofibromatosis
• A Solitary Intestinal Myofibroma: A Rare Cause of Neonatal Anemia
• A tyrosine kinase-activating variant Asn666Ser in PDGFRB causes a progeria-like condition in the severe end of Penttinen syndrome
• A Unique Case of Multicentric Infantile Myofibromatosis with Radiologic-Pathologic Correlation
• A Unique Presentation of Multicentric Myofibromatosis in the Masseter Muscle of a Pediatric Patient
• Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapy
• Adult-Onset Multifocal Cutaneous Myofibromas: A Case Report of a Rare Entity
• Aggressive infantile myofibromatosis with intestinal involvement
• An unusual case of a solitary cardiac myofibroma causing severe right ventricular outflow tract obstruction in an infant
• Association of PDGFRB Mutations With Pediatric Myofibroma and Myofibromatosis
• Avoidance of surgery for head and neck infantile myofibromatosis using imatinib monotherapy
• Clinical utility of vinblastine therapeutic drug monitoring for the treatment of infantile myofibroma patients: A case series
• Congenital Infantile Fibrosarcoma Involving Pelvic Wall and Thigh Soft Tissues and Placenta, Presenting with Coagulopathy
• Congenital Infantile Myofibroma: The Importance of Molecular Diagnosis
• Congenital Myofibroblastic Skin Tumours in a Newborn Piglet Resembling the Multicentric Form of Infantile Myofibromatosis
• Corneal Infantile Myofibromatosis Caused by Novel Activating Imatinib-Responsive Variants in <em>PDGFRB</em>
• Corneal Infantile Myofibromatosis Caused by Novel Activating Imatinib-Responsive Variants in PDGFRB
• Diagnostic limitations and considerations in the imaging evaluation of advanced multicentric infantile myofibromatosis
• Diverse presentation and tailored treatment of infantile myofibromatosis: A single-center experience
• Effects of Sunitinib and Other Kinase Inhibitors on Cells Harboring a <em>PDGFRB</em> Mutation Associated with Infantile Myofibromatosis
• Effects of Sunitinib and Other Kinase Inhibitors on Cells Harboring a PDGFRB Mutation Associated with Infantile Myofibromatosis
• Evaluation of pan-TRK immunohistochemistry in infantile fibrosarcoma, lipofibromatosis-like neural tumour and histological mimics
• Expansion of the phenotype of Kosaki overgrowth syndrome
• Extended Endonasal Endoscopic Complete Resection of a Solitary Intraorbital Myofibroma: A Case Report and Literature Review
• Fibroblastic and myofibroblastic tumors of children: new genetic entities and new ancillary testing
• Firm digital papulonodules in a young boy
• Generalized Infantile Myofibromatosis with Extensive Small Bowel Involvement in a Neonate
• Generalized infantile myofibromatosis with visceral involvement presenting as diffuse hypopigmented macules at birth
• Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working Group
• Genomic analysis reveals germline and somatic PDGFRB variants with clinical implications in familial infantile myofibromatosis
• Giant intracranial infantile myofibromatosis of the skull base: report of two cases
• Gynecology and Oncology Fetal Myofibromatosis: A Challenge for Prenatal Diagnosis Mini Review of the English Literature
• Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile Myofibromatosis
• Infantile myofibromatosis
• Infantile myofibromatosis - a clinical and pathological diagnostic challenge
• Infantile myofibromatosis in a 5-month-old boy
• Infantile Myofibromatosis of the Femoral Neck: A Case Report
• Infantile myofibromatosis of the iliac bone
• Infantile myofibromatosis treated by mandibulectomy and staged reconstruction with submental flap and free fibula flap: a case report
• Infantile Myofibromatosis With Cutaneous, Visceral, and CNS Involvement: A Multimodal Approach to Therapy
• Infantile Myofibromatosis With Intracranial Extradural Involvement and PDGFRB Mutation: A Case Report and Review of the Literature
• Infantile Myofibromatosis: 32 Patients and Review of Literature
• Infantile myofibromatosis: a rare cause of subcutaneous nodules in an infant
• Infantile myofibromatosis: Excellent prognosis but also rare fatal progressive disease. Treatment results of five Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry
• Infantile myofibromatosis: multiple firm nodules in a premature newborn
• Infantile myofibromatosis: review of imaging findings and emphasis on correlation between MRI and histopathological findings
• Intralesional 5-Fluorouracil: A Therapy for Solitary Infantile Myofibromatosis
• Isolated infantile myofibroma of the calvarium: Report of a case with a literature review
• Kosaki overgrowth syndrome: A novel pathogenic variant in PDGFRB and expansion of the phenotype including cerebrovascular complications
• Late Relapse in Genetically Determined Infantile Myofibromatosis. A Case Report and Brief Focus on Recurrences
• Left mandibular infantile myofibromatosis: a case report
• Major response to imatinib and chemotherapy in a newborn patient prenatally diagnosed with generalized infantile myofibromatosis
• Massive infantile myofibromatosis of the upper lip causing airway distress in a newborn
• Multicentric infantile myofibromatosis with extensive involvement limited to bone
• Multiple firm erythematous nodules on the scalp of a child
• Multiple skin nodules in a newborn
• Myofibromatosis presenting as reticulated vascular changes and subcutaneous atrophy in a patient with somatic mosaicism of PDGFRB mutation
• Myopericytomatosis: Clinicopathologic Analysis of 11 Cases With Molecular Identification of Recurrent PDGFRB Alterations in Myopericytomatosis and Myopericytoma
• Neurofibromatosis 1 in the setting of dual diagnosis: Diagnostic and management conundrums
• Non-malignant fibroblastic/myofibroblastic tumors in pediatric age group: Clues and pitfalls to the cytological diagnosis
• Notch Pathway and Inherited Diseases: Challenge and Promise
• Novel <em>PDGFRB</em> rearrangement in multifocal infantile myofibromatosis is tumorigenic and sensitive to imatinib
• Novel Aspects of Genetics, Molecular Biology and Clinical Oncology of Sarcomas
• Novel COL4A1-VEGFD gene fusion in myofibroma
• Novel Oncogenic <em>PDGFRB</em> Variant in Severe Infantile Myofibromatosis With Response to Imatinib Using Therapeutic Drug Monitoring
• Novel Oncogenic PDGFRB Variant in Severe Infantile Myofibromatosis With Response to Imatinib Using Therapeutic Drug Monitoring
• Novel PDGFRB rearrangement in multifocal infantile myofibromatosis is tumorigenic and sensitive to imatinib
• PDGF receptor mutations in human diseases
• PDGFRB and NOTCH3 Mutations are Detectable in a Wider Range of Pericytic Tumors, Including Myopericytomas, Angioleiomyomas, Glomus Tumors, and Their Combined Tumors
• PDGRFB mutation-associated myofibromatosis: Response to targeted therapy with imatinib
• Pearls and Pitfalls in the Imaging of Soft-Tissue Masses in Children
• Pediatric myofibroma/myofibromatosis of the soft tissue and bone: a clinicopathological analysis of 28 cases
• Penttinen syndrome-associated PDGFRB Val665Ala variant causes aberrant constitutive STAT1 signalling
• Prenatal genetic diagnosis of disseminated infantile myofibromatosis: a case report and literature review
• Prenatal imaging patterns of different forms of infantile myofibromatosis
• Prenatal sonography of multicentric infantile myofibromatosis: Case report and review of the literature
• Prenatally Diagnosed Infantile Myofibroma of Sartorius Muscle-A Differential for Soft Tissue Masses in Early Infancy
• Primary Resection and Immediate Autologous Reconstruction of Fronto-orbital Infantile Myofibromatoses
• Proportion of children with cancer that have an indication for genetic counseling and testing based on the cancer type irrespective of other features
• Proptosis secondary to infantile myofibromatosis in a newborn: role of the ophthalmologist from diagnosis to treatment
• Segmental overgrowth and aneurysms due to mosaic PDGFRB p.(Tyr562Cys)
• Solitary cutaneous infantile myofibroma as a hallmark of myofibromatosis: Two cases and review of the literature
• Solitary infantile myofibromatosis in the upper extremities: Case report
• Solitary infantile myofibromatosis of the petrous bone: a diagnostic pitfall in uncommon location illustrated by a case report
• Solitary myofibroma preceding the development of multicentric myofibromatosis: A report of two cases with surveillance recommendations
• Spontaneous involution (regression) of a solitary cutaneous myofibroma in an adult patient
• Sporadic infantile myofibromatosis: Mutations with PDGFRB gain-of-function
• Sternocleidomastoid size and upper trapezius muscle thickness in congenital torticollis patients: A retrospective observational study
• The developmental biology of genetic Notch disorders
• The infantile myofibromatosis NOTCH3 L1519P mutation leads to hyperactivated ligand-independent Notch signaling and increased PDGFRB expression
• The Master of Puppets: Pleiotropy of PDGFRB and its Relationship to Multiple Diseases
• Treatment of generalized infantile myofibromatosis with sorafenib and imatinib: A case report
• Unresectable infantile myofibroma discovered in utero
• Utility of 18F-FDG PET/CT in Infantile Myofibromatosis
• What to Look Out for in a Newborn with Multiple Papulonodular Skin Lesions at Birth
• Whole-body magnetic resonance imaging in the diagnosis and follow-up of multicentric infantile myofibromatosis: A case report