365 related articles for article (PubMed ID: 19015486)
1. Early-onset dementia with prolonged occipital seizures: an atypical case of Kufs disease.
Zini A; Cenacchi G; Nichelli P; Zunarelli E; Todeschini A; Meletti S
Neurology; 2008 Nov; 71(21):1709-12. PubMed ID: 19015486
[TBL] [Abstract][Full Text] [Related]
2. [A case of adult neuronal ceroid lipofuscinosis type A].
Fujita N; Kimura T; Matsubara N; Tabe H; Tanaka K
Rinsho Shinkeigaku; 1999 Apr; 39(4):478-80. PubMed ID: 10391979
[TBL] [Abstract][Full Text] [Related]
3. The problematic issue of Kufs disease diagnosis as performed on rectal biopsies: a case report.
Pasquinelli G; Cenacchi G; Piane EL; Russo C; Aguglia U
Ultrastruct Pathol; 2004; 28(1):43-8. PubMed ID: 14967598
[TBL] [Abstract][Full Text] [Related]
4. New subform of the late infantile form of neuronal ceroid lipofuscinosis.
Wisniewski KE; Kida E; Connell F; Elleder M; Eviatar L; Konkol RJ
Neuropediatrics; 1993 Jun; 24(3):155-63. PubMed ID: 8355821
[TBL] [Abstract][Full Text] [Related]
5. [A 54-year-old man with action myoclonus, parkinsonism and epilepsy].
Yoshioka A; Saiki S; Yamaya Y; Kanemoto M; Hirose G
No To Shinkei; 1999 Nov; 51(11):999-1007. PubMed ID: 10586420
[TBL] [Abstract][Full Text] [Related]
6. [Adult neuronal ceroid lipofuscinosis (Kufs disease)--a rare cause of dementia].
Kozian R; Kiszka T; Peter K
Psychiatr Prax; 1994 Nov; 21(6):235-7. PubMed ID: 7824670
[TBL] [Abstract][Full Text] [Related]
7. [Clinical and electroencephalographic aspects of late infantile neuronal ceroid lipofuscinosis].
Caraballo R; Sologuestua A; Ruggieri VL; Monges S; Cersósimo R; Taratuto AL; Medina C; Fejerman N
Rev Neurol; 2005 Feb 1-15; 40(3):135-40. PubMed ID: 15750896
[TBL] [Abstract][Full Text] [Related]
8. Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations.
Striano P; Specchio N; Biancheri R; Cannelli N; Simonati A; Cassandrini D; Rossi A; Bruno C; Fusco L; Gaggero R; Vigevano F; Bertini E; Zara F; Santorelli FM; Striano S
Epilepsy Behav; 2007 Feb; 10(1):187-91. PubMed ID: 17129765
[TBL] [Abstract][Full Text] [Related]
9. Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features.
Berkovic SF; Oliver KL; Canafoglia L; Krieger P; Damiano JA; Hildebrand MS; Morbin M; Vears DF; Sofia V; Giuliano L; Garavaglia B; Simonati A; Santorelli FM; Gambardella A; Labate A; Belcastro V; Castellotti B; Ozkara C; Zeman A; Rankin J; Mole SE; Aguglia U; Farrell M; Rajagopalan S; McDougall A; Brammah S; Andermann F; Andermann E; Dahl HM; Franceschetti S; Carpenter S
Brain; 2019 Jan; 142(1):59-69. PubMed ID: 30561534
[TBL] [Abstract][Full Text] [Related]
10. [Dementia and psychiatric disorders in Kufs disease].
Charles N; Vighetto A; Pialat J; Confavreux C; Aimard G
Rev Neurol (Paris); 1990; 146(12):752-6. PubMed ID: 2291038
[TBL] [Abstract][Full Text] [Related]
11. Neurological progress. The neuronal ceroid lipofuscinoses: a review.
Boustany RM; Kolodny EH
Rev Neurol (Paris); 1989; 145(2):105-10. PubMed ID: 2657976
[TBL] [Abstract][Full Text] [Related]
12. [Dementia following bipolar disorder].
Lebert F; Lys H; Haëm E; Pasquier F
Encephale; 2008 Dec; 34(6):606-10. PubMed ID: 19081458
[TBL] [Abstract][Full Text] [Related]
13. [Clinico-pathological investigation of two patients with dementia with motor neuron disease].
Yamamoto R; Iseki E; Murayama N; Minegishi M; Kimura M; Eto K; Arai H; Ohbu S; Hatanaka D; Hino H; Fujisawa K
Brain Nerve; 2007 Mar; 59(3):263-9. PubMed ID: 17370652
[TBL] [Abstract][Full Text] [Related]
14. [Klüver-Bucy syndrome as the initial symptom of adult-type ceroid lipofuscinosis (Kufs' disease)].
Alonso-Navarro H; Jiménez-Jiménez FJ; Puertas-Muñoz I; Rábano J; de Yébenes JG; Sarasa-Corral JL
Rev Neurol; 2005 Jan 16-31; 40(2):93-8. PubMed ID: 15712163
[TBL] [Abstract][Full Text] [Related]
15. Adult neuronal ceroid lipofuscinosis presenting with psychiatric symptoms: a case report.
Augustine A; Fricchione G; Woznicki R; Broberg D; Holt J
Int J Psychiatry Med; 1993; 23(4):315-22. PubMed ID: 8175244
[TBL] [Abstract][Full Text] [Related]
16. Autosomal dominant Kufs' disease: a cause of early onset dementia.
Josephson SA; Schmidt RE; Millsap P; McManus DQ; Morris JC
J Neurol Sci; 2001 Jul; 188(1-2):51-60. PubMed ID: 11489285
[TBL] [Abstract][Full Text] [Related]
17. Progressive myoclonic epilepsy: A clinical, electrophysiological and pathological study from South India.
Sinha S; Satishchandra P; Gayathri N; Yasha TC; Shankar SK
J Neurol Sci; 2007 Jan; 252(1):16-23. PubMed ID: 17166519
[TBL] [Abstract][Full Text] [Related]
18. Novel compound heterozygous mutations causing Kufs disease type B.
Wang C; Xu H; Yuan Y; Lian Y; Xie N; Ming L
Int J Neurosci; 2018 Jun; 128(6):573-576. PubMed ID: 29120254
[TBL] [Abstract][Full Text] [Related]
19. Evaluation of 36 patients from Turkey with neuronal ceroid lipofuscinosis: clinical, neurophysiological, neuroradiological and histopathologic studies.
Topçu M; Tan H; Yalnizoğlu D; Usubütün A; Saatçi I; Aynaci M; Anlar B; Topaloğlu H; Turanli G; Köse G; Aysun S
Turk J Pediatr; 2004; 46(1):1-10. PubMed ID: 15074367
[TBL] [Abstract][Full Text] [Related]
20. FAME 3: a novel form of progressive myoclonus and epilepsy.
Carr JA; van der Walt PE; Nakayama J; Fu YH; Corfield V; Brink P; Ptacek L
Neurology; 2007 Apr; 68(17):1382-9. PubMed ID: 17452583
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]