Atrial Fibrillation < Atrophy < Atropine

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 153.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000026 (1999)	E. Marchioni [Italie] ; D. Soragna ; M. Versino ; L. Sibilla ; E. Alfonsi ; A. Romani ; R. Manni ; F. Savoldi	Hemiparkinsonism-hemiatrophy with brain hemihypoplasia.
000282 (2000)	E H Aylward [États-Unis] ; A M Codori ; A. Rosenblatt ; M. Sherr ; J. Brandt ; O C Stine ; P E Barta ; G D Pearlson ; C A Ross	Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease.
000349 (2000)	L. Vercueil [France] ; A. Hammouti ; M L Andriantseheno ; M. Mohr ; C. Tranchant ; P. Maquet ; C. Marescaux ; F. Sellal	Pallido-Luysio-Nigral atrophy revealed by rapidly progressive hemidystonia: a clinical, radiologic, functional, and neuropathologic study.
000468 (2001)	B V Manyam [États-Unis] ; A S Walters ; K R Narla	Bilateral striopallidodentate calcinosis: clinical characteristics of patients seen in a registry.
000477 (2001)	J M Henderson [Australie] ; W P Gai ; M A Hely ; W G Reid ; G L Walker ; G M Halliday	Parkinson's disease with late Pick's dementia.
000485 (2001)	C. Chuang [Royaume-Uni] ; R S Kocen ; N P Quinn ; S E Daniel	Case with both multiple system atrophy and primary progressive multiple sclerosis with discussion of the difficulty in their differential diagnosis.
000486 (2001)	J A Van Gerpen [États-Unis]	Camptocormia secondary to early amyotrophic lateral sclerosis.
000491 (2001)	J. Müller [Autriche] ; G K Wenning ; J. Wissel ; Werner Poewe [Autriche]	Intrafamilial heterogeneity of facial hyperkinesias: chance association of tics, cranial dystonia, and Huntington's disease?
000528 (2001)	J H Friedman [États-Unis] ; N. Shetty	Permanent cerebellar toxicity of cytosine arabinoside (Ara C) in a young woman.
000541 (2001)	N J Cordato [Australie] ; G M Halliday ; H. Mccann ; L. Davies ; P. Williamson ; M. Fulham ; J G Morris	Corticobasal syndrome with tau pathology.
000671 (2002)	Kin-Lun Tsang [Royaume-Uni] ; Susan Daniel ; Rick Stell ; Peter Brown ; Niall Quinn	Sixty-six-year-old woman with unexplained falls followed five years later by severe generalized myoclonus.
000744 (2002)	Pierre-François Pradat [France] ; François Salachas ; Lucette Lacomblez ; Nathalie Patte ; Nadine Leforestier ; Véronique Gaura ; Vincent Meininger	Association of chorea and motor neuron disease.
000907 (2002)	Chin-Song Lu [Taïwan] ; Yah-Huei Wu Chou ; Tzu-Chen Yen ; Chon-Haw Tsai ; Rou-Shayn Chen ; Hsiu-Chen Chang	Dopa-responsive parkinsonism phenotype of spinocerebellar ataxia type 2.
000964 (2002)	Michael R. Pranzatelli [États-Unis] ; Elizabeth D. Tate ; Marcel Kinsbourne ; Verne S. Caviness ; Bibhuti Mishra	Forty-one year follow-up of childhood-onset opsoclonus-myoclonus-ataxia: cerebellar atrophy, multiphasic relapses, and response to IVIG.
000977 (2003)	Ram N C. Leiguarda [Argentine] ; Marcelo Merello ; María Inés Nouzeilles ; Jorge Balej ; Alberto Rivero ; Martín Nogués	Limb-kinetic apraxia in corticobasal degeneration: clinical and kinematic features.
000A07 (2003)	Carsten Buhmann [Allemagne] ; Alexandra Bussopulos ; Matthias Oechsner	Dopaminergic response in Parkinsonian phenotype of Machado-Joseph disease.
000A37 (2003)	Saeed Bohlega [Arabie saoudite] ; Adel Al-Jishi ; Carol Dobson-Stone ; Luca Rampoldi ; Parthasarathi Saha ; Hatem Murad ; Abid Kareem ; George Roberts ; Anthony P. Monaco	Chorea-acanthocytosis: clinical and genetic findings in three families from the Arabian peninsula.
000A47 (2003)	Neil Mahant [Australie] ; Dennis J. Cordato ; Victor S C. Fung	Focal myoclonus-dystonia of the leg secondary to a lesion of the posterolateral putamen: clinical and neurophysiological features.
000A49 (2003)	Melih Vural [Turquie] ; Sibel Ozekmekçi ; Hülya Apaydin ; Attila Altinel	High-dose piracetam is effective on cerebellar ataxia in patient with cerebellar cortical atrophy.
000A68 (2003)	Edith Werber [Israël] ; Colin Klein ; Jonathan Grünfeld ; José Martin Rabey	Phenotypic presentation of frontotemporal dementia with Parkinsonism-chromosome 17 type P301S in a patient of Jewish-Algerian origin.
000A98 (2003)	Richard Camicioli [États-Unis] ; M Milar Moore ; Anthony Kinney ; Elizabeth Corbridge ; Kathryn Glassberg ; Jeffrey A. Kaye	Parkinson's disease is associated with hippocampal atrophy.

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