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 |
---|
000162 (2006) |
Birgül Azrak [Allemagne] ; Kristina Kaevel ; Ludwig Hofmann ; Christiane Gleissner ; Brita Willershausen | Dystrophic epidermolysis bullosa: Oral findings and problems |
000280 (2003) |
| Posters |
000407 (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 |
000614 (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 |
000653 (1905) |
| THE BRITISH MEDICAL ASSOCIATION. |
000A32 (1966) |
C B Kerr ; R S Wells ; K E Cooper | Gene effect in carriers of anhidrotic ectodermal dysplasia. |
001916 (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 |
001F71 (1972) |
Merton Ian Satinoff [Royaume-Uni] | The medical biology of the early Egyptian populations from Asswan, Assyut and Gebelen |
002687 (1969) |
P. K. Misra ; P. C. Bajpai | Anhidrotic hereditary ectodermal dysplasia in four generations |
002F17 (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 |
003076 (2002) |
| Poster session 7: Ataxia, chorea, drug‐induced movement disorders, myoclonus, spasticity, stereotypies, tics, tremor |
003372 (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 |
004A41 (1978) |
Anna-Maija Raeste [Finlande] ; Y. Collan [Finlande] ; E. Kilpinen [Finlande] | Hereditary fibrous hyperplasia of the gingiva with varying penetrance and expressivity |
004D16 (1977) |
B. M. Tress [Royaume-Uni] ; I. F. Moseley [Royaume-Uni] | Cleidocranial dysostosis, hereditary haemorrhagic telangiectasia and epilepsy: A rare association |
004E96 (2004) |
Bart Post [Pays-Bas] ; Johannes H. T. M. Koelman [Pays-Bas] ; Marina A. J. Tijssen [Pays-Bas] | Propriospinal myoclonus after treatment with ciprofloxacin |
005312 (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 |
005464 (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 |
005470 (1923) |
| Literature |
005621 (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 |
005627 (1957) |
Milton B. Asbell [États-Unis] | A study of the family-line transmission of dental occlusion |
005788 (1975) |
J B Familusi ; F. Jaiyesimi ; C O Ojo ; E B Attah | Herediatary anhidrotic ectodermal dysplasia. Studies in a Nigerian famil. |
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