PAPERS - RESEARCH FRONT: 14
TITLE	1ST AUTHOR	YEAR
[F-18] FDG PET IN FATAL FAMILIAL INSOMNIA - THE FUNCTIONAL-EFFECTS OF THALAMIC LESIONS	PERANI D	1993
A NOTE ON FATAL FAMILIAL INSOMNIA	HUMANES JFN	1994
DIURNAL BLOOD-PRESSURE VARIATION AND HORMONAL CORRELATES IN FATAL FAMILIAL INSOMNIA	PORTALUPPI F	1994
FATAL FAMILIAL INSOMNIA - SLEEP, NEUROENDOCRINE AND VEGETATIVE ALTERATIONS	MONTAGNA P	1995
SLEEP-WAKE CYCLE ABNORMALITIES IN FATAL FAMILIAL INSOMNIA - EVIDENCE OF THE ROLE OF THE THALAMUS IN SLEEP REGULATION	SFORZA E	1995
Fatal familial insomnia: Behavioral and cognitive features	Gallassi R	1996
Thalamic form of Creutzfeldt-Jakob disease or fatal insomnia? Report of a sporadic case with normal prion protein genotype	Kawasaki K	1997
Biopsy diagnosis of Creutzfeldt-Jakob disease by western blot: A case report	Castellani RJ	1997
Cerebral metabolism in fatal familial insomnia: Relation to duration, neuropathology, and distribution of protease-resistent prion protein	Cortelli P	1997
The D178N (cis-129M) ''fatal familial insomnia'' mutation associated with diverse clinicopathologic phenotypes in an Australian kindred	McLean CA	1997
Familial spongiform encephalopathy associated with a novel prion protein gene mutation	Nitrini R	1997
Diffuse thalamic degeneration in fatal familial insomnia. A morphometric study	Macchi G	1997
Fatal familial insomnia - Genetic, neuropathologic, and biochemical study of a patient from a new Italian kindred	Rossi G	1998
Clinical features of fatal familial insomnia: Phenotypic variability in relation to a polymorphism at codon 129 of the prion protein gene	Montagna P	1998
Molecular pathology of fatal familial insomnia	Parchi P	1998
Conclusions of the Symposium	Gambetti P	1998
Fatal familial insomnia in a new Italian kindred	Padovani A	1998
Fatal familial insomnia: clinical features and molecular genetics	Cortelli P	1999
A subtype of sporadic prion disease mimicking fatal familial insomnia	Parchi P	1999
Novel twelve-generation kindred of fatal familial insomnia from Germany representing the entire spectrum of disease expression	Harder A	1999
Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia	Parchi P	2000
Sleep disorders associated to prion diseases	Merino-Ramirez MA	2000
Alteration of the serotonergic nervous system in fatal familial insomnia	Wanschitz J	2000
Gerstmann-Straussier-Scheinker syndrome, fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies	Collins S	2001
Serial positron emission tomographic findings in an atypical presentation of fatal familial insomnia	Bar KJ	2002
Familial and sporadic fatal insomnia	Montagna P	2003
Early age of onset in fatal familial insomnia - Two novel cases and review of the literature	Harder A	2004
Fatal familial insomnia with an unusual prion protein deposition pattern: an autopsy report with an experimental transmission study	Sasaki K	2005
Sporadic fatal insomnia with spongiform degeneration in the thalamus and widespread PrPSc deposits in the brain	Piao YS	2005