Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated with IGF1 Mutation Demonstrates Its Critical Role in Growth and Brain Development
NaspäťBibliografické údaje
- Rok vydania
- 2009
- Kategória
- ADC — Vedecké práce v zahraničných karentovaných časopisoch
- CREPČ / EPCA ID
- 0009174
- Typ dokumentu
- Článok z periodika
- Zdroj
- Journal of Clinical Endocrinology and Metabolism
- ISSN (Zdroj)
- 0021-972X
- Zväzok
- Vol. 94, č. 10 (2009), s. 3913-3921
- Jazyk
- anglický
Bibliografický zápis
NETCHINE, Iréne - AZZI, Salah - HOUANG, Muriel - SEURIN, Danielle - PERIN, Laurence - RICORT, Jean-Marc - DAUBAS, Claudine - LEGAY, Christine - MEŠTER, Ján - HERICH, Róbert - GODEAU, François - LE BOUC, Yves. Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated with IGF1 Mutation Demonstrates Its Critical Role in Growth and Brain Development. In: Journal of Clinical Endocrinology and Metabolism. 2009. ISSN 0021-972X, Vol. 94, č. 10 (2009), s. 3913-3921. (2009: 6.202 - IF, 343 - H-index, 6.46 - IF 5y, 3.225 - SJR, Q1 - SJR Best Q, Q1 - JCR Best Q, 1.833 - ABDC).
Autori publikácie
| Autor | Rola | Podiel |
|---|---|---|
| Iréne Netchine | Autor | 0.000 % |
| Salah Azzi | Autor | 0.000 % |
| Muriel Houang | Autor | 0.000 % |
| Danielle Seurin | Autor | 0.000 % |
| Laurence Perin | Autor | 0.000 % |
| Jean-Marc Ricort | Autor | 0.000 % |
| Claudine Daubas | Autor | 0.000 % |
| Christine Legay | Autor | 0.000 % |
| Ján Mešter | Autor | 0.000 % |
| Róbert Herich | Autor | 0.000 % |
| François Godeau | Autor | 0.000 % |
| Yves Le Bouc | Autor | 0.000 % |
Metriky
Ohlasy (98)
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|---|---|---|
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SCOPUS |
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WOS |
| 2025 1 |
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WOS |
| 2024 1 |
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| 2024 1 |
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