Serveur d'exploration sur le patient édenté - Checkpoint (Istex)

Index « Teeft.i » - entrée « Hereditary »
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List of bibliographic references

Number of relevant bibliographic references: 29.
[0-20] [0 - 20][0 - 29][20-28][20-40]
Ident.Authors (with country if any)Title
000650 (2013) L. Nibali [Royaume-Uni] ; A. Medlar [Royaume-Uni] ; H. Stanescu [Royaume-Uni] ; R. Kleta [Royaume-Uni] ; U. Darbar [Royaume-Uni] ; N. Donos [Royaume-Uni]Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis
002C77 (2006) Birgül Azrak [Allemagne] ; Kristina Kaevel ; Ludwig Hofmann ; Christiane Gleissner ; Brita WillershausenDystrophic epidermolysis bullosa: Oral findings and problems
002F94 (2005) K. Kavvadia [Grèce] ; E. Pepelassi ; C. Alexandridis ; A. Arkadopoulou ; G. Polyzois ; K. Tossios [Grèce]Gingival fibromatosis and significant tooth eruption delay in an 11‐year‐old male: a 30‐month follow‐up
003130 (2004) Christoph Schrader [Allemagne] ; Thomas Peschel [Allemagne] ; Michael Petermeyer [Allemagne] ; Reinhard Dengler [Allemagne] ; Dieter Hellwig [Allemagne]Unilateral deep brain stimulation of the internal globus pallidus alleviates tardive dyskinesia
003162 (2004) Renato P. Munhoz [Canada] ; Catherine Bergeron [Canada] ; Anthony E. Lang [Canada]Sporadic case of dentatorubral pallidoluysian atrophy with no CAG repeat expansion and no intranuclear inclusions
003170 (2004) John Yianni [Royaume-Uni] ; Dipankar Nandi [Royaume-Uni] ; Kevin Bradley [Royaume-Uni] ; Nigel Soper [Royaume-Uni] ; Ralph Gregory [Royaume-Uni] ; Carole Joint [Royaume-Uni] ; John Stein [Royaume-Uni] ; Richard Scott [Royaume-Uni] ; Tipu Aziz [Royaume-Uni]Senile chorea treated by deep brain stimulation—A clinical, neurophysiological and functional imaging study
003173 (2004) Alastair Wilkins [Royaume-Uni] ; Jerry M. Brown [Royaume-Uni] ; Roger A. Barker [Royaume-Uni]SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report
003188 (2004) Bart Post [Pays-Bas] ; Johannes H. T. M. Koelman [Pays-Bas] ; Marina A. J. Tijssen [Pays-Bas]Propriospinal myoclonus after treatment with ciprofloxacin
003300 (2004) Yih-Ru Wu [Taïwan] ; Guey-Jen Lee-Chen [Taïwan] ; Anthony E. Lang [Canada] ; Chiung-Mei Chen [Taïwan] ; Hsuan-Yuan Lin [Taïwan] ; Sien-Tsong Chen [Taïwan]Dystonia as a presenting sign of spinocerebellar ataxia type 1
003315 (2004) Birgit Herting [Allemagne] ; Silke Wunderlich [Allemagne] ; Theresa Glöckler [Allemagne] ; Martin Bendszus [Allemagne] ; Dirk Mucha [Allemagne] ; Heinz Reichmann [Allemagne] ; Markus Naumann [Allemagne]Computed tomographically‐controlled injection of botulinum toxin into the longus colli muscle in severe anterocollis
003356 (2004) Akio Kikuchi [Japon] ; Atsushi Takeda [Japon] ; Kazuo Fujihara [Japon] ; Teiko Kimpara [Japon] ; Yusei Shiga [Japon] ; Hiroaki Tanji [Japon] ; Makiko Nagai [Japon] ; Hiroshi Ichinose [Japon] ; Fumi Urano [Japon] ; Nobuyuki Okamura [Japon] ; Hiroyuki Arai [Japon] ; Yasuto Itoyama [Japon]Arg(184)his mutant GTP cyclohydrolase I, causing recessive hyperphenylalaninemia, is responsible for dopa‐responsive dystonia with parkinsonism: A case report
003511 (2003) Posters
003816 (2002) Poster session 7: Ataxia, chorea, drug‐induced movement disorders, myoclonus, spasticity, stereotypies, tics, tremor
004592 (1998) Anne B. Jonkman ; Anne B. Pas ; Anne B. Fine [États-Unis]Mosaic expression of uncein, linear IgA bullous dermatosis antigen and 180‐kDa bullous pemphigoid antigen in generalized atrophic benign epidermolysis bullosa
005E67 (1985) Audrey Heimler [États-Unis] ; James Sciubba [États-Unis] ; Ernest Lieber [États-Unis] ; Saul Kamen [États-Unis]An unusual presentation of opalescent dentin and Brandywine isolate hereditary opalescent dentin in an Ashkenazic Jewish family
006723 (1978) Anna-Maija Raeste [Finlande] ; Y. Collan [Finlande] ; E. Kilpinen [Finlande]Hereditary fibrous hyperplasia of the gingiva with varying penetrance and expressivity
006808 (1977) B. M. Tress [Royaume-Uni] ; I. F. Moseley [Royaume-Uni]Cleidocranial dysostosis, hereditary haemorrhagic telangiectasia and epilepsy: A rare association
006943 (1975) J B Familusi ; F. Jaiyesimi ; C O Ojo ; E B AttahHerediatary anhidrotic ectodermal dysplasia. Studies in a Nigerian famil.
006980 (1974) Twenty five year cumulative index
006A84 (1972) Merton Ian Satinoff [Royaume-Uni]The medical biology of the early Egyptian populations from Asswan, Assyut and Gebelen
006C93 (1969) P. K. Misra ; P. C. BajpaiAnhidrotic hereditary ectodermal dysplasia in four generations

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