Works matching DE "ENCHONDROMATOSIS"

Results: 67

Characteristics of gliomas in patients with somatic IDH mosaicism.

Published in:

Acta Neuropathologica Communications, 2016, v. 4, p. 1, doi. 10.1186/s40478-016-0302-y

By:

Bonnet, Charlotte;
Thomas, Laure;
Psimaras, Dimitri;
Bielle, Franck;
Vauléon, Elodie;
Loiseau, Hugues;
Cartalat-Carel, Stéphanie;
Meyronet, David;
Dehais, Caroline;
Honnorat, Jérôme;
Sanson, Marc;
Ducray, François

Publication type:

Article

Paediatric chondrosarcomas: a retrospective review of 17 cases.

Published in:

Histopathology, 2016, v. 68, n. 7, p. 1073, doi. 10.1111/his.12881

By:

Gambarotti, Marco;
Righi, Alberto;
Picci, Piero;
Bertoni, Franco;
Manfrini, Marco;
Donati, Davide M;
Dei Tos, Angelo P;
Vanel, Daniel

Publication type:

Article

Mutations in IDH1 and IDH2 are not present in sporadic ovarian sex cord-stromal tumours.

Published in:

Histopathology, 2015, v. 66, n. 6, p. 897, doi. 10.1111/his.12489

By:

Aitken, Sarah J;
Presneau, Nadège;
Khatri, Bhavisha;
Flanagan, Adrienne M;
Clarke, Blaise;
McCluggage, W Glenn

Publication type:

Article

Ollier Disease, Acute Myeloid Leukemia, and Brain Glioma: IDH as the Common Denominator.

Published in:

Cancers, 2024, v. 16, n. 18, p. 3125, doi. 10.3390/cancers16183125

By:

Corvino, Sergio;
Somma, Teresa;
Certo, Francesco;
Bonomo, Giulio;
Grasso, Erica;
Esposito, Felice;
Berardinelli, Jacopo;
Barbagallo, Giuseppe

Publication type:

Article

Brain Gliomas and Ollier Disease: Molecular Findings as Predictive Risk Factors?

Published in:

Cancers, 2022, v. 14, n. 14, p. N.PAG, doi. 10.3390/cancers14143464

By:

Corvino, Sergio;
Mariniello, Giuseppe;
Corazzelli, Giuseppe;
Franca, Raduan Ahmed;
Del Basso De Caro, Marialaura;
Della Monica, Rosa;
Chiariotti, Lorenzo;
Maiuri, Francesco

Publication type:

Article

Congenital and metabolic disorders leading to fracture.

Published in:

Trauma, 2012, v. 14, n. 3, p. 243, doi. 10.1177/1460408611434391

By:

Borland, Steven;
Gaffey, Andrew

Publication type:

Article

A case of early onset renal sarcoidosis complecated with multiple enchondromatosis.

Published in:

2011

By:

Kaneko, U.;
Toyabe, S.;
Uchiyama, M.

Publication type:

Abstract

Multiple Enchondromatosis: Ollier's Disease.

Published in:

JK Science, 2010, v. 12, n. 4, p. 207

By:

Shaheen, Feroze;
Ahmad, Nisar;
Gojwari, Tariq;
Teli, M. Ashraf;
Resold, Riyaz;
Singh, Manjeet

Publication type:

Article

Do Glioblastomas with Syndromic Association Have Better Prognosis? A Case of Supratentorial Glioblastoma with Embryonal Tumor Differentiation in a Child with Multiple Enchondromatosis.

Published in:

Journal of Pediatric Neurosciences, 2019, v. 14, n. 4, p. 228, doi. 10.4103/jpn.JPN_82_19

By:

Vankipuram, Siddharth;
Sahoo, Sushant;
Bhalla, Shalini;
Srivastava, Chittij

Publication type:

Article

MR Features of Multiple Enchondromas with Associated Chondrosarcoma in the Lower Extremities.

Published in:

2016

By:

Kyung Yoon Yang;
Mi Sook Sung;
Won Jong Yu;
Hee Jeong Lee;
Il Joong Park;
Jae Young Lee;
Gook Jin Lee;
Sang Hoon Jeon;
Mi Na Yu;
Se Cheol Yoon

Publication type:

Case Study

Effective sirolimus treatment for refractory spindle cell haemangioma.

Published in:

British Journal of Dermatology, 2018, v. 179, n. 4, p. 976, doi. 10.1111/bjd.16739

By:

Ho, C.B.;
Chiou, J.F.;
Lee, H.L.;
Hsieh, K.;
Chen, W.Y.;
Lin, Y.T.;
Shiah, H.S.

Publication type:

Article

Maffucci syndrome with the spindle cell hemangiomas in the mucosa of the lower lip: a rare case report and literature review.

Published in:

Journal of Cutaneous Pathology, 2013, v. 40, n. 7, p. 661, doi. 10.1111/cup.12131

By:

Cai, Yu;
Wang, Rong;
Chen, Xin‐Ming;
Zhao, Yi‐Fang;
Sun, Zhi‐Jun;
Zhao, Ji‐Hong

Publication type:

Article

Maffucci syndrome and neoplasms: a case report and review of the literature.

Published in:

2016

By:

Prokopchuk, Olga;
Andres, Stephanie;
Becker, Karen;
Holzapfel, Konstantin;
Hartmann, Daniel;
Friess, Helmut

Publication type:

Case Study

Enchondroma of the skull base secondary to generalized enchondromatosis: A case report and review of the literature.

Published in:

ENT: Ear, Nose & Throat Journal, 2011, v. 90, n. 11, p. 535, doi. 10.1177/014556131109001101.1

By:

Rogers, Derek J.;
Boseley, Mark E.;
Stephan, Mark J.;
Browd, Samuel;
Semerad, David C.

Publication type:

Article

Enchondroma of the nasal septum due to Ollier disease: A case report and review of the literature.

Published in:

Head & Neck, 2015, v. 37, n. 3, p. E30, doi. 10.1002/hed.23783

By:

Jacobi, Christian M. C.;
Hiranya, Egodage Samitha;
Gay, Annietta;
Holzmann, David;
Kollias, Spyridon;
Soyka, Michael B.;
Irish, Jonathan

Publication type:

Article

Sclerosing angiomatoid nodular transformation of the spleen in a patient with Maffucci syndrome: a case report and review of literature.

Published in:

Diagnostic Pathology, 2017, v. 12, p. 1, doi. 10.1186/s13000-017-0670-z

By:

Xiao-Dan Huang;
Hao-Sen Jiao;
Zheng Yang;
Chuang-Qi Chen;
Yu-Long He;
Xin-Hua Zhang

Publication type:

Article

MAFFUCCI'S SYNDROME ASSOCIATED WITH HYPERPARATHYROIDISM.

Published in:

Indian Journal of Dermatology, 2011, v. 56, n. 2, p. 195, doi. 10.4103/0019-5154.80418

By:

Rao, Angoori Gnaneshwar;
Indira, Danturty;
Rekha, Tulja Narsing

Publication type:

Article

Differential Diagnosis of Cartilaginous Lesions of Bone.

Published in:

Archives of Pathology & Laboratory Medicine, 2020, v. 144, n. 1, p. 71, doi. 10.5858/arpa.2019-0441-RA

By:

Suster, David;
Yin Pun Hung;
Nielsen, G. Petur

Publication type:

Article

Multifocal intracranial astrocytoma in a pediatric patient with Ollier disease.

Published in:

Indian Journal of Radiology & Imaging, 2012, v. 22, n. 1, p. 58, doi. 10.4103/0971-3026.95406

By:

Bathla, Girish;
Gupta, Sarika;
Cheng, Kang Ong

Publication type:

Article

Genetics: IDH mosaicism in enchondromatosis syndromes.

Published in:

2012

By:

Alderton, Gemma K.

Publication type:

journal article

A rare differential diagnosis of multiple swellings: Maffucci's syndrome: case report and review of literature.

Published in:

International Journal of Students' Research, 2011, v. 1, n. 4, p. 133

By:

Pathak, Ritesh Suresh;
Prasad, D. V.

Publication type:

Article

ASYMPTOMATIC SIX YEAR OLD GIRL WITH MULTIPLE BONY SWELLINGS.

Published in:

2016

By:

Ahmed, Minhajuddin;
Ali, Manal Ashraf

Publication type:

Case Study

HAND INVOLVEMENT IN OLLIER DISEASE AND MAFFUCCI SYNDROME: A CASE SERIES.

Published in:: Acta Reumatológica Portuguesa, 2010, v. 35, n. 3, p. 375
Publication type:: Article

Chondrosarcoma of the nasal cavity in a patient with Maffucci syndrome: case report and review of the literature.

Published in:

2014

By:

Steinbichler, Teresa;
Kral, Florian;
Reinold, Susanne;
Riechelmann, Herbert

Publication type:

Case Study

Exostosis múltiple hereditaria. Reporte de un caso y diagnóstico diferencial de las encondromatosis.

Published in:

Acta Ortopédica Mexicana, 2012, v. 26, n. 6, p. 388

By:

Cammarata-Scalisi, F.;
Sánchez-Flores, R.;
Stock-Leyton, F.;
Labrador-Chacón, N.;
Cammarata-Scalisi, G.

Publication type:

Article

Encondromatosis múltiple familiar, diagnóstico diferencial: presentación de un caso clínico con condrosarcoma y revisión de la literatura.

Published in:

Acta Ortopédica Mexicana, 2009, v. 23, n. 6, p. 376

By:

Sansón-RíoFrío, J. A.;
Santiesteban, S. Navarro;
Bahena, R. I.;
Villavicencio, V. V.;
Martínez-Said, H.;
Padilla, R. A.;
Cuellar, H. M.

Publication type:

Article

Granulosa-Cell Tumor Diagnosed in the Third Decade of Life in a Patient with Ollier's Disease: A Rare But Clinically Important Correlation.

Published in:

Journal of Gynecologic Surgery, 2023, v. 39, n. 1, p. 53, doi. 10.1089/gyn.2022.0042

By:

Hughes-Hogan, Logan;
Popiolek, Dorota;
Duncan, Karen;
Timor-Tritsch, Ilan E.

Publication type:

Article

Chondrosarcoma of the chest wall with Ollier's disease.

Published in:

1998

By:

Yaldız, S.;
Başok, O.;
Ülğan, M.;
Karadağ, T.;
Gürsoy, S.;
Bayol, Ü.;
Yaldiz, S;
Başok, O;
Ulğan, M;
Karadağ, T;
Gürsoy, S;
Bayol, U

Publication type:

journal article

Maffucci syndrome in a 10-year- old boy.

Published in:

2011

By:

NUTAN, FNU

Publication type:

Case Study

Juvenile granulosa cell tumor associated with Ollier disease.

Published in:

Skeletal Radiology, 2023, v. 52, n. 3, p. 605, doi. 10.1007/s00256-022-04033-5

By:

Littrell, Laurel A.;
Inwards, Carrie Y.;
Hazard, Florette K.;
Wenger, Doris E.

Publication type:

Article

Update on the imaging features of the enchondromatosis syndromes.

Published in:

Skeletal Radiology, 2022, v. 51, n. 4, p. 747, doi. 10.1007/s00256-021-03870-0

By:

Sharif, Ban;
Lindsay, Daniel;
Saifuddin, Asif

Publication type:

Article

Widespread and debilitating hemangiomas in a patient with enchondromatosis and D-2-hydroxyglutaric aciduria.

Published in:

2018

By:

Yeetong, Patra;
Phewplung, Teerasak;
Kamolvisit, Wuttichart;
Suphapeetiporn, Kanya;
Shotelersuk, Vorasuk

Publication type:

journal article

Juvenile granulosa cell tumor associated with Ollier disease.

Published in:

Indian Journal of Medical & Paediatric Oncology, 2016, v. 37, n. 4, p. 293, doi. 10.4103/0971-5851.195749

By:

Sampagar, Abhilasha Ashok;
Jahagirdar, Rahul R.;
Bafna, Vibha Sanjay;
Bartakke, Sandip P.

Publication type:

Article

Bone scintigraphy in Ollier's disease: A rare case report.

Published in:

Indian Journal of Nuclear Medicine, 2013, v. 28, n. 4, p. 226, doi. 10.4103/0972-3919.121968

By:

Khan, Shoukat H.;
Rather, Tanveer A.;
Koul, Parvaiz A.;
Makhdoomi, Rumana;
Bhat, Abdul Rashid;
Malik, Dharmender;
Manohar, Ram

Publication type:

Article

IDH1 immunohistochemistry reactivity and mosaic IDH1 or IDH2 somatic mutations in pediatric sporadic enchondroma and enchondromatosis.

Published in:

2019

By:

Saiji, Essia;
Pause, Fabienne Gumy;
Lascombes, Pierre;
Cerato Biderbost, Christelle;
Marq, Nathalie Lin;
Berczy, Margaret;
Merlini, Laura;
Rougemont, Anne-Laure

Publication type:

journal article

Different appearance of Ollier disease: enchondromatosis of the ribs.

Published in:

2017

By:

Candas, Fatih;
Yildizhan, Akin;
Gorur, Rauf

Publication type:

Other

Maffucci Syndrome.

Published in:

Bulletin of the Hospital for Joint Diseases, 2015, v. 73, n. 4, p. 282

By:

Ngai, Calvin;
Ding, David Y.;
Rapp, Timothy B.

Publication type:

Article

Ovarian cellular fibroma harbouring an isocitrate dehydrogenase 1 ( 1 DH1) mutation in a patient with Ollier disease: evidence for a causal relationship.

Published in:

Histopathology, 2013, v. 62, n. 4, p. 667, doi. 10.1111/his.12054

By:

Kenny, Sarah L;
Patel, Kaushik;
Humphries, Anna;
Davis, Michael;
Flanagan, Adrienne M;
McCluggage, W Glenn

Publication type:

Article

Relapsing-Remitting Sixth Nerve Palsy in Association with Ollier's Disease.

Published in:

Neuro-Ophthalmology, 2015, v. 39, n. 2, p. 92, doi. 10.3109/01658107.2014.998772

By:

Raoof, Naz;
Batty, Ruth;
Carroll, Thomas A.;
Pepper, Irene M.;
Sandison, Ann;
Eckersley, Rupert;
Hickman, Simon J.

Publication type:

Article

Ollier’s Disease of the Iliac Bone with Sacroiliac Joint Involvement in an Adolescent Patient.

Published in:

Case Reports in Surgery, 2016, p. 1, doi. 10.1155/2016/4893718

By:

Savvidou, Olga D.;
Chloros, George D.;
Koutsouradis, Panagiotis;
Skarpidi, Evangelia;
Papagelopoulos, Panayiotis J.

Publication type:

Article

Maffucci's Syndrome or a Variant?

Published in:

APSP Journal of Case Reports, 2013, v. 4, n. 2, p. 1

By:

Yousuf Aziz Khan;
Soofia Ahmad

Publication type:

Article

Ollier's disease associated with ovarian juvenile granulosa cell tumor and triple X syndrome: A letter to the editor.

Published in:

Journal of Research in Medical Sciences, 2022, v. 27, n. 5, p. 41, doi. 10.4103/jrms.jrms_980_21

By:

Shafieyoon, Shamim;
Tahririan, Mohammad;
Hekmatnia, Ali;
Zarei, Andrew;
Hekmatnia, Farzaneh;
Soufi, Ghazaleh

Publication type:

Article

Ollier Disease.

Published in:

Applied Radiology, 2023, v. 52, n. 4, p. 36, doi. 10.37549/ar2912

By:

Morgan, Daniel;
Towbin, Richard B.;
Towbin, Alexander J.

Publication type:

Article

Ollier’s disease.

Published in:

Applied Radiology, 2014, v. 43, n. 1, p. 34, doi. 10.37549/ar2139

By:

Kitley, Charles A.;
Reidman, Daniel A.;
Balingit, Antonio G.

Publication type:

Article

Somatic IDH1 variant (p.R132C) in an adult male with Maffucci syndrome.

Published in:

2021

By:

Brown, Natasha J.;
Zimeng Ye;
Stutterd, Chloe;
Jayasinghe, Sureshni I.;
Schneider, Amy;
Mullen, Saul;
Mandelstam, Simone A.;
Hildebrand, Michael S.

Publication type:

Case Study

Ollier Disease and a Case of Prolonged Menstrual Bleeding in an 11-Year-Old Girl: What's the Missing Link?

Published in:

2022

By:

Kaneta, Kelli;
Khalighi, Misha;
Borzutzky, Claudia;
Bhatia, Parul

Publication type:

Case Study

Ollier disease with anaplastic astrocytoma: A review of the literature and a unique case.

Published in:

2016

By:

Gajavelli, Srikanth;
Nakhla, Jonathan;
Nasser, Rani;
Yassari, Reza;
Weidenheim, Karen M.;
Graber, Jerome

Publication type:

Case Study

A Case of Enchondromatosis Concomitant with Cerebral Hamartomas: Radiologic Findings.

Published in:

Fetal & Pediatric Pathology, 2011, v. 30, n. 2, p. 111, doi. 10.3109/15513815.2010.524689

By:

Avcu, Serhat;
Çetin, Feray;
Ünal, Özkan

Publication type:

Article

Limb lengthening for deformities in Ollier's disease: a systematic review.

Published in:

European Journal of Orthopaedic Surgery & Traumatology, 2020, v. 30, n. 8, p. 1325, doi. 10.1007/s00590-020-02692-5

By:

Angelini, Andrea;
Baracco, Riccardo;
Dolci, Andrea;
Vigo, Marco;
Mavrogenis, Andreas F.;
Ruggieri, Pietro

Publication type:

Article

Venous malformation: update on aetiopathogenesis, diagnosis and management.

Published in:

Phlebology, 2010, v. 25, n. 5, p. 224, doi. 10.1258/phleb.2009.009041

By:

Dompmartin, A.;
Vikkula, M.;
Boon, L. M.

Publication type:

Article