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Nature Genetics, ISSN 1061-4036, 12/2011, Volume 43, Issue 12, pp. 1256 - 1261
Journal Article
Journal Article
INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY, ISSN 0378-6323, 05/2019, Volume 85, Issue 3, pp. 291 - 294
Maffucci syndrome is a rare nonhereditary disorder comprising of lymphovascular malformations and multiple enchondromas, which may be associated with several... 
synovial sarcoma | Enchondroma | lymphangioma | VARIANT | Maffucci syndrome | DERMATOLOGY | Dysplasia | Bone diseases | Diagnosis | Research | Case studies | Tissue | Vein & artery diseases | Tumors
Journal Article
Medecine Nucleaire, ISSN 0928-1258, 05/2017, Volume 41, Issue 3, pp. 204 - 204
Journal Article
Eplasty, ISSN 1937-5719, 2014, Volume 14, p. ic11
Journal Article
Indian journal of anaesthesia, ISSN 0019-5049, 05/2019, Volume 63, Issue 5, pp. 400 - 402
Maffucci syndrome is an extremely rare, sporadic, and nonhereditary disease characterized by enchondromatosis, bony abnormalities, and vascular malformations.... 
Vecuronium | Parathyroid hormone | Anesthesia | Case studies | Care and treatment | Usage | Bone tumors | Anesthetics | Fractures | Scoliosis | Surgery | Bones | Larynx | Intubation | Patients | Tumors | Deformities | enchondromas | maffucci | haemangiomas | Case Report
Journal Article
World Neurosurgery, ISSN 1878-8750, 10/2019, Volume 130, pp. e356 - e361
Maffucci syndrome (MS) and Ollier disease (OD) are rare diseases characterized by multiple benign enchondromas. The incidence of skull base (SB) enchondromas... 
Maffucci | Chondrosarcoma | Transformation | Enchondroma | Ollier | Skull base | CT imaging | Diagnostic imaging | Seizures (Medicine)
Journal Article
Periodontology 2000, ISSN 0906-6713, 06/2019, Volume 80, Issue 1, pp. 12 - 27
Journal Article
WORLD NEUROSURGERY, ISSN 1878-8750, 10/2019, Volume 130, pp. E356 - E361
BACKGROUND: Maffucci syndrome (MS) and Oilier disease (OD) are rare diseases characterized by multiple benign enchondromas. The incidence of skull base (SB)... 
GLIOMAS | SURGERY | Chondrosarcoma | Transformation | Skull base | Enchondroma | Oilier | OLLIERS-DISEASE | TUMORS | CLINICAL NEUROLOGY | Maffucci | EMPHASIS | ABC/2 | PATIENT | BONE | OF-THE-LITERATURE | BRAIN | RADIOLOGY
Journal Article
Indian Journal of Otolaryngology and Head & Neck Surgery, ISSN 2231-3796, 10/2019, Volume 71, Issue S1, pp. 652 - 656
Maffucci syndrome is an extremely rare sporadic disease, characterized by multiple enchondromas and associated with multiple hemangiomas and/or lymphangiomas.... 
Enchondromas | Medicine & Public Health | Maffucci syndrome | Head and Neck Surgery | Otorhinolaryngology | Nasopharynx | Chondrosacomas | Surveillance | Mutation
Journal Article
Surgical Pathology Clinics, ISSN 1875-9181, 06/2016, Volume 9, Issue 2, pp. 269 - 287
This review covers gynecologic manifestations that may occur in rare hereditary syndromes. Recent advances in disorders, such as hereditary leiomyomatosis,... 
Cowden syndrome | Maffucci syndrome | Hereditary leiomyomatosis renal cell carcinoma syndrome | Tuberous sclerosis | Von Hippel-Lindau | Ollier disease | Carney complex | Nevoid basal cell carcinoma syndrome | Neoplastic Syndromes, Hereditary - pathology | Prognosis | Uterine Neoplasms - pathology | Humans | Lymphangioleiomyomatosis - pathology | Carney Complex - pathology | von Hippel-Lindau Disease - diagnosis | Genital Neoplasms, Female - diagnosis | Tuberous Sclerosis - pathology | Basal Cell Nevus Syndrome - pathology | von Hippel-Lindau Disease - pathology | Leiomyomatosis - diagnosis | Skin Neoplasms - diagnosis | Carney Complex - genetics | Leiomyomatosis - pathology | Female | Neoplastic Syndromes, Hereditary - genetics | Tuberous Sclerosis - diagnosis | Uterine Neoplasms - diagnosis | Carney Complex - diagnosis | Genital Neoplasms, Female - genetics | Skin Neoplasms - pathology | Uterine Neoplasms - genetics | Diagnosis, Differential | Hamartoma Syndrome, Multiple - genetics | Hamartoma Syndrome, Multiple - pathology | Basal Cell Nevus Syndrome - diagnosis | Neoplastic Syndromes, Hereditary - diagnosis | von Hippel-Lindau Disease - genetics | Enchondromatosis - diagnosis | Tuberous Sclerosis - genetics | Perivascular Epithelioid Cell Neoplasms - pathology | Hamartoma Syndrome, Multiple - diagnosis | Perivascular Epithelioid Cell Neoplasms - genetics | Skin Neoplasms - genetics | Basal Cell Nevus Syndrome - genetics | Enchondromatosis - pathology | Leiomyomatosis - genetics | Perivascular Epithelioid Cell Neoplasms - diagnosis | Genital Neoplasms, Female - pathology | Enchondromatosis - genetics | Lymphangioleiomyomatosis - diagnosis | Lymphangioleiomyomatosis - genetics
Journal Article
Dermatologic Therapy, ISSN 1396-0296, 05/2019, Volume 32, Issue 3, pp. e12919 - n/a
Maffucci syndrome is a rare genetic disease due to somatic mutation of IDH1 gene. Currently there is no medical treatment available for spindle cell hemangioma... 
spindle cell hemangioma | IDH 1 mutation | Maffucci syndrome | sirolimus | RAPAMYCIN | HEMANGIOENDOTHELIOMAS | MUTATIONS | VARIANT | DERMATOLOGY | Hemangioma | Care and treatment
Journal Article
PATHOLOGE, ISSN 0172-8113, 05/2017, Volume 38, Issue 3, pp. 179 - 185
Journal Article
Journal Article