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Publication Date:
October 2003
ISSN:
2191-0367

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International Journal on Disability and Human Development

Official journal of the the National Institute of Child Health and Human Development in Israel

Editor-in-Chief: Merrick, Joav

Editorial Board Member: Brooks, Tony / Carmeli, Eli / Dalton, Arthur J / Davidson, Philip W / Galil, Ahron / Heller, Tamar / Huff, Marlene B. / Janicki, Matthew P. / Kerr, Mike / Levy, Howard B / Lindström, Bengt / Morad, Mohammed / Omar, Hatim A. / Prasher, Vee / Shek, Daniel T.L. / Sher, Leo / Stratakis, Constantine A / Postolache, Teodor T.

4 Issues per year

Increased IMPACT FACTOR 2011: 0.300

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Issues

Ahead of print >

Volume 12 (2013)

Volume 11 (2012)

Volume 10 (2011)

Volume 9 (2010)

Volume 8 (2009)

Volume 7 (2008)

Volume 6 (2007)

Volume 5 (2006)

Volume 4 (2005)

Volume 3 (2003)

Volume 2 (2001)

Volume 1 (2000)

Most Downloaded Articles

  1. Masthead
  2. Cognitive profile of patients with alcoholic Korsakoff's syndrome by Brand , Matthias
  3. A screening battery for the assessment of executive functioning in young and adult individuals with intellectual disability by Sgaramella, Teresa M./ Carrieri, Loredana and Barone, Caterina
  4. Acute alcohol-induced impairment of cognitive functions: Past and present findings by Fillmore , Mark Τ
  5. Future of integrative medicine: A view from the United States by Kemper , Kathi J

Issue 3-4 (Oct 2003), pp. 101 - 172

CONTENTS

Page I

Letter from the Editor

Page 101

Obituary - Dr. Jean Pierre Luton (1933-2002)

Page 103

Role of the Transcription Factor CREB (cAMP Response Element Binding Protein) in Endocrine Tissue Development and Tumorigenesis

Rosenberg , D. / Groussin , L. / Cazabat , L. / Jullian , E. / René-Corail , F. / Bertagna , X. / Bertherat , J.

Page 105

The Genetics of Autoimmune Thyroid Disease

Kacem , H. Hadj / Rebai , A. / Ayadi , H. / Farid , N.R.

Page 115

A Novel Insertional Mutation in the Mu-Opioid Receptor Gene is Associated with Altered Cortisol Response to Naloxone

Salvatori , R. / Yang , X. / Wand , G.

Page 129

Mutations in the TTF2 Gene are Not a Common Finding in Patients with Isolated Cleft Palate and Choanal Atresia

Venza , M. / Santarpia , L. / De Ponte , F. Saverio / D'Alcontres , F. Stagno / Teti , D. / Benvenga , S.

Page 135

Effect of Exogenous Insulin-like Growth Factor-I (IGF-I) on the Expression of the IGF-I Gene and the Genes of IGF-Binding Proteins (IGFBPs) 1-4 in Human Thyroid Cells from Nodular Goiter, Follicular Adenoma and Follicular Carcinoma Cultured in Monolayers

Lewinski , A. / Marcinkowska , M. / Brzeziańska , E. / Tantush , A.S. / Wloch , J. / Brzeziński , J.

Page 141

Mutation of FGFR3 in a Patient with Craniosynostosis, Hypochondroplasia and Growth Hormone Deficiency

Coco , M. / Mattina , T. / Mancuso , M. / Zingale , A. / Baffico , M. / Caruso-Nicoletti , M.

Page 151

Clinical, Genetic and Endocrine Aspects of a Patient with 45,X/48,XYYY Mosaicism: Patient Report and Review of the Literature

Francisco , J.L. Ruibal / Rodríguez , O. Pérez / Soriano , B. Nievas / Medina , L. Ortega / Pérez , C. Cotarelo / Ecenarro , M.J. Lautre

Page 157

No Evidence for a Role of Genomic Variants in CIT1 in the Etiology of Silver-Russell Syndrome

Meyer , E. / Wollmann , H.A. / Eggermann , T.

Page 161

BOOK REVIEWS. CALENDAR. INDEX

Page 165

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