List of bibliographic references indexed by Autosomal
Number of relevant bibliographic references: 57.
[20-40] [
0 - 20][
0 - 50][
40-56][
40-60]
| Ident. | Authors (with country if any) | Title |
|---|
| 007914 (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 |
| 007929 (2004) |
Bart Post [Pays-Bas] ; Johannes H. T. M. Koelman [Pays-Bas] ; Marina A. J. Tijssen [Pays-Bas] | Propriospinal myoclonus after treatment with ciprofloxacin |
| 007987 (2004) |
Angelo Mariotti | Laboratory testing of patients with systemic conditions in periodontal practice |
| 007A41 (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 |
| 007A56 (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 |
| 007A97 (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 |
| 008424 (2002) |
| Poster session 7: Ataxia, chorea, drug‐induced movement disorders, myoclonus, spasticity, stereotypies, tics, tremor |
| 008935 (2001) |
Bishakha Rajagopalan [Australie] | Non‐bullous ichthyosiform erythroderma associated with retinitis pigmentosa |
| 008975 (2001) |
Joerg Meyle ; José R. Gonzáles | Influences of systemic diseases on periodontitis in children and adolescents |
| 008996 (2001) |
Penny Hodge ; Bryan Michalowicz | Genetic predisposition to periodontitis in children and young adults |
| 008997 (2001) |
Rudolf Happle [Allemagne] | Genetic hair loss |
| 008A47 (2001) |
M. Kozakiewicz [Pologne] ; W. Perczynska-Partyka [Pologne] ; J. Kobos [Pologne] | Cherubism—clinical picture and treatment |
| 009861 (1998) |
Frédéric Bernard ; Jean-Laurent Casanova ; Giulia Cournot ; Nada Jabado ; Jane Peake ; Sébastien Jauliac ; Alain Fischer ; Claire Hivroz | The protein tyrosine kinase p60c-Src is not implicated in the pathogenesis of the human autosomal recessive form of osteopetrosis: A study of 13 children |
| 009930 (1998) |
André Mégarbané [Liban] ; Ziad Noujeim [Liban] ; Michel Fabre [France] ; Vazken M. Der Kaloustian [Canada] | New form of hidrotic ectodermal dysplasia in a Lebanese family |
| 009C73 (1997) |
Thomas J. Borris ; Timothy Bandrowsky ; Andrew A. Vorono | Vestibuloplasty with a split thickness skin graft in a patient with ehlers-danlos syndrome |
| 009D66 (1997) |
William J. Craigen [États-Unis] ; Moise L. Levy [États-Unis] ; And Richard A. Lewis [États-Unis] | Schöpf‐Schulz‐Passarge syndrome with an unusual pattern of inheritance |
| 009E53 (1997) |
Hans Peter M. Freihofer [Pays-Bas] ; Sajjad Walji [Pays-Bas] ; Han G. Brunner [Pays-Bas] | Ectodermal dysplasia, cleft lip/palate, and severe cutaneous and osseous syndactyly in a mentally retarded girl: A new multiple malformation syndrome |
| 00A338 (1996) |
Eric A. Wulfsberg [États-Unis] ; Andrew B. Campbell [États-Unis] ; Iosif W. Lurie [États-Unis] ; Karen R. Eanet [États-Unis] | Confirmation of the catania brachydactylous type of acrofacial dysostosis: Report of a second family |
| 00AE01 (1993) |
J. Bollerslev [Danemark, États-Unis] ; S. C. Marks Jr. [États-Unis] ; S. Pockwinse [États-Unis] ; M. Kassem [Danemark] ; K. Brixen [Danemark] ; T. Steiniche [Danemark] ; L. Mosekilde [Danemark] | Ultrastructural investigations of bone resorptive cells in two types of autosomal dominant osteopetrosis |
| 00AE61 (1993) |
Robert J. Genco [États-Unis] ; Harald Löe [États-Unis] | The role of systemic conditions and disorders in periodontal disease |
| 00B651 (1991) |
Jeppe Gram [Danemark] ; Steen Antonsen [Danemark] ; Mogens H Rder [Danemark] ; Jens Bollerslev [Danemark] | Elevated serum levels of creatine kinase BB in autosomal dominant osteopetrosis type II |
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