Alawaji O, Aweja G
Cureus. 2024; 16(6):e62076.
PMID: 38989390
PMC: 11235393.
DOI: 10.7759/cureus.62076.
Monjaras-Romo G, Zavala-Romero L, Fernanda Tejada-Pineda M, Meraz-Soto J, Ballesteros-Herrera D, Cienfuegos-Meza J
Cureus. 2023; 15(8):e44326.
PMID: 37779805
PMC: 10536449.
DOI: 10.7759/cureus.44326.
Kolhe A, Shenoy A, Tayal S, Goel N
J Neurosci Rural Pract. 2023; 14(1):127-131.
PMID: 36891111
PMC: 9944648.
DOI: 10.25259/JNRP-2022-3-10.
Fotakopoulos G, Brotis A, Paterakis K, Kapsalaki E, Fountas K
Asian J Neurosurg. 2022; 17(4):680-682.
PMID: 36570746
PMC: 9771626.
DOI: 10.1055/s-0042-1757433.
Cheng C, Ou C, Chen J, Lui C, Yeh L
Radiol Case Rep. 2019; 14(6):734-739.
PMID: 30988866
PMC: 6447731.
DOI: 10.1016/j.radcr.2019.03.020.
Lhermitte-Duclos disease : (Diffuse cerebellar hypertrophy) prolonged post-operative survival.
Banerjee A, Gleadhill C
Ir J Med Sci. 2016; 148(1):97.
PMID: 27517397
DOI: 10.1007/BF02938059.
Lhermitte-Duclos Disease: Diagnosis on MRI, MR Spectroscopy, CT and Positron Emission Tomography.
Jain N, Chauhan U, Goel V, Puri S
J Clin Diagn Res. 2015; 9(9):TJ01-2.
PMID: 26500979
PMC: 4606308.
DOI: 10.7860/JCDR/2015/13840.6517.
Assessing a dysplastic cerebellar gangliocytoma (Lhermitte-Duclos disease) with 7T MR imaging.
Moenninghoff C, Kraff O, Schlamann M, Ladd M, Katsarava Z, Gizewski E
Korean J Radiol. 2010; 11(2):244-8.
PMID: 20191074
PMC: 2827790.
DOI: 10.3348/kjr.2010.11.2.244.
A developmental and genetic classification for midbrain-hindbrain malformations.
Barkovich A, Millen K, Dobyns W
Brain. 2009; 132(Pt 12):3199-230.
PMID: 19933510
PMC: 2792369.
DOI: 10.1093/brain/awp247.
Cowden syndrome: a critical review of the clinical literature.
Pilarski R
J Genet Couns. 2008; 18(1):13-27.
PMID: 18972196
DOI: 10.1007/s10897-008-9187-7.
Lhermitte-Duclos disease.
Kumar R, Vaid V, Kalra S
Childs Nerv Syst. 2007; 23(7):729-32.
PMID: 17221273
DOI: 10.1007/s00381-006-0271-8.
Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults.
Zhou X, Marsh D, Morrison C, Chaudhury A, Maxwell M, Reifenberger G
Am J Hum Genet. 2003; 73(5):1191-8.
PMID: 14566704
PMC: 1180498.
DOI: 10.1086/379382.
Dysplastic gangliocytoma (Lhermitte-Duclos disease) associated with Cowden disease: report of a case and review of the literature for the genetic relationship between the two diseases.
Murata J, Tada M, Sawamura Y, Mitsumori K, Abe H, Nagashima K
J Neurooncol. 1999; 41(2):129-36.
PMID: 10222433
DOI: 10.1023/a:1006167421100.
Lhermitte-Duclos disease associated with syringomyelia.
Marcus C, Galeon M, Peruzzi P, Bazin A, Bernard M, Pluot M
Neuroradiology. 1996; 38(6):529-31.
PMID: 8880711
DOI: 10.1007/BF00626089.
Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?.
Eng C, Murday V, Seal S, Mohammed S, Hodgson S, Chaudary M
J Med Genet. 1994; 31(6):458-61.
PMID: 8071972
PMC: 1049923.
DOI: 10.1136/jmg.31.6.458.
Association of Lhermitte-Duclos and Cowden disease: report of a new case and review of the literature.
Vinchon M, Blond S, Lejeune J, Krivosik I, Fossati P, Assaker R
J Neurol Neurosurg Psychiatry. 1994; 57(6):699-704.
PMID: 8006650
PMC: 1072973.
DOI: 10.1136/jnnp.57.6.699.
Dysplastic gangliocytoma of the cerebellum (Lhermitte-Duclos disease) and its relation to the multiple hamartoma syndrome (Cowden disease).
Rimbau J, ISAMAT F
J Neurooncol. 1994; 18(3):191-7.
PMID: 7964980
DOI: 10.1007/BF01328953.
An adult patient with cerebellar ganglioglioma.
Handa H, Yamagami T, Furuta M
J Neurooncol. 1994; 18(3):183-9.
PMID: 7525889
DOI: 10.1007/BF01328952.
Lhermitte-Duclos disease (diffuse hypertrophy of the cerebellum). Report of two cases.
Gessaga E
Neurosurg Rev. 1980; 3(2):151-8.
PMID: 7231686
DOI: 10.1007/BF01644067.
Lhermitte-Duclos disease.
REZNIK M, Schoenen J
Acta Neuropathol. 1983; 59(2):88-94.
PMID: 6837278
DOI: 10.1007/BF00691592.