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Publication Date:
April 1999
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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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. An exploratory study of patient interventions and nutritional advice for patients with chronic obstructive pulmonary disease, living in the community by Dickinson, Jill

Issue 2 (Apr 1999), pp. 59 - 112

CONTENTS

Page I

Letter from the Editors

Page 59

Glucocorticoid Receptor Isoforms Alpha and Beta: Potential Physiological and Pathological Importance

Vottero , A. / Chrousos , G.P.

Page 61

NeuroD/Beta2 Polymorphism is Not Associated with Type 1 Diabetes in Chinese, Korean, or Caucasian Populations

Marron , M.P. / Hopkins , D.I. / Park , Y.S. / She , J.-X.

Page 73

CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient

De Carvalho , C.E. / Penachioni , J.Y. / Castro , M. / Moreira , A.C. / De Mello , M.P.

Page 79

Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes

Gill-Randall , R. / Evans , L. / Alcolado , J.C.

Page 87

A Novel Mutation (W718S) in the Steroid-Binding Domain of the Androgen Receptor Gene in a Boy with Ambiguous Genitalia and Hypergonadotrophic Hypogonadism

Ribeiro , M.L. / Cabral , D.F. / Maciel-Guerra , A.T. / Guerra Jr. , G. / Hackel , C.

Page 91

Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene

Tiulpakov , A.N. / Orlovsky , I.V. / Kalintchenko , N.U. / Lonina , D.A. / Kalesnikova , G.S. / Peterkova , V.A. / Bjamason , R. / Baumbach , L. / Rubtsov , P.M.

Page 95

Homozygous Transthyretin Leu64: A Very Rare Transthyretin Mutation Associated With Amyloidosis but Not With Euthyroid Hyperthyroxinemia

Benvenga , S. / Bartolone , L. / Musolino , R. / Melluso , R. / Toscano , A. / Vita , G. / Trimarchi , F.

Page 101

FORUM AND CORRESPONDENCE. BOOK REVIEWS. CALENDAR

Page 105

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