International Journal on Disability and Human Development

1

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.

Journal:

Year:

2003

Language:

english

File:

PDF, 1.61 MB

english, 2003

2

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

Journal:

International Journal on Disability and Human Development

Year:

2003

Language:

english

File:

PDF, 127 KB

english, 2003

4

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.

Journal:

International Journal on Disability and Human Development

Year:

2003

Language:

english

File:

PDF, 1.33 MB

english, 2003

5

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

Journal:

International Journal on Disability and Human Development

Year:

2003

Language:

english

File:

PDF, 484 KB

english, 2003

6

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.

Journal:

International Journal on Disability and Human Development

Year:

2003

Language:

english

File:

PDF, 678 KB

english, 2003

7

BOOK REVIEWS. CALENDAR. INDEX

Journal:

International Journal on Disability and Human Development

Year:

2003

Language:

english

File:

PDF, 1002 KB

english, 2003

8

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.

Journal:

International Journal on Disability and Human Development

Year:

2003

Language:

english

File:

PDF, 622 KB

english, 2003

9

The Genetics of Autoimmune Thyroid Disease

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

Journal:

International Journal on Disability and Human Development

Year:

2003

Language:

english

File:

PDF, 2.11 MB

english, 2003

10

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

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

Journal:

International Journal on Disability and Human Development

Year:

2003

Language:

english

File:

PDF, 658 KB

english, 2003

11

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

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

Journal:

International Journal on Disability and Human Development

Year:

2003

Language:

english

File:

PDF, 439 KB

english, 2003

12

Letter from the Editor

Journal:

International Journal on Disability and Human Development

Year:

2003

Language:

english

File:

PDF, 75 KB

english, 2003

Volume 3; Issue 3-4

International Journal on Disability and Human Development

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

CONTENTS

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

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

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

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

BOOK REVIEWS. CALENDAR. INDEX

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

The Genetics of Autoimmune Thyroid Disease

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

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

Letter from the Editor