JOURNAL OF
PEDIATRIC
ENDOCRINOLOGY & METABOLISM
VOLUME 22, NUMBER 3
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MARCH 2009
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EDITORIAL |
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Are the Statistics We Are
Reading Correct? |
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Z. Zadik, Rehovot,
Israel [free text] |
193 |
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REVIEW |
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The Use of Surrogate Vascular Markers in Youth
at Risk for Premature Cardiovascular Disease |
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C.J. McNeal,
D.P. Wilson, D. Christou, R.L. Bush, L.G. Shepherd, J. Santiago and G.Y. Wu, Temple
and College Station,
TX, USA [free text] |
195 |
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IMAGES IN PEDIATRIC ENDOCRINOLOGY |
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Neonatal Escherichia coli
Meningitis can be Complicated by Central Permanent Diabetes Insipidus |
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J. Baruteau, A. Cartault, A.
Chanot, A. Sevely and C. Casper, Toulouse, France [free
text] |
213 |
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ORIGINAL CONTRIBUTIONS
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Arginine and Clonidine
Stimulation Tests for Growth Hormone Deficiency Revisited – Do We Really Need So Many
Samples? |
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L. Muster, D.H. Zangen,
R. Nesher, H.J. Hirsch, Z. Muster and D. Gillis, Jerusalem, Israel |
215 |
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Insulin-like Growth Factor-I,
Insulin-like Growth Factor Binding Protein-3 and Growth in Obese Children Before and
After Reduction of Overweight |
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T. Reinehr, A.
Panteliadou, G. de Sousa and W. Andler, Datteln, Germany |
225 |
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Hand Size and Growth in
Untreated and IGF-I Treated Patients with Laron Syndrome |
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O. Konen, A. Silbergeld,
P. Lilos, L. Kornreich and Z. Laron, Tel Aviv, Israel |
235 |
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Vitamin D Nutritional Status of Exclusively
Breast Fed Infants and Their Mothers |
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A. Seth, R.K. Marwaha, B. Singla, S.
Aneja, P. Mehrotra, A. Sastry, M.L. Khurana, K. Mani, B. Sharma and N. Tandon, New Delhi, India |
241 |
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Genetic Analysis of the SRD5A2 Gene in Indian Patients with 5a-Reductase Deficiency |
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R. Sahu, R. Boddula, P.
Sharma, V. Bhatia, R. Greaves, S. Rao, M. Desai, A. Wakhlu, S. Phadke, M.
Shukla, P. Dabadghao, R.N. Mehrotra
and E. Bhatia, Lucknow,Mumbai and Hyderabad, India and Parkville,
Victoria, Australia |
247 |
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Hydrocortisone Treatment in
Girls with Congenital Adrenal Hyperplasia Inhibits Serum Dehydroepiandrosterone
Sulfate and Affects the GH–IGF-I System |
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G. Guercio, M.A.
Rivarola, E. Chaler, M. Maceiras and A. Belgorosky, Buenos Aires,
Argentina |
255 |
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PATIENT REPORT LETTERS |
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Unusual Thyroid Constellation in Down
Syndrome: Congenital Hypothyroidism, Graves’ Disease, and Hemiagenesis in the Same Child |
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T.D. Nebesio and E.A.
Eugster, Indianapolis, IN, USA |
263 |
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Activating TSH-Receptor Mutation
(Met453Thr) as a Cause of Adenomatous Non-Autoimmune Hyperthyroidism in a 3 Year-old Boy |
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S. Kraemer, K. Rothe, R. Pfaeffle, D.
Fuehrer-Sakel, H. Till and O.J. Muensterer, Leipzig, Germany |
269 |
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Mother-to-Son Transmission of a
Luteinizing Hormone Receptor Activating Mutation in a Prepubertal Child with Testotoxicosis |
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M. Eunice, P. Philibert, B. Kulshreshtha,
F. Audran, F. Paris, C. Sultan and A.C. Ammini, New Delhi, India and
Montpellier, France |
275 |
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Recurrence of Giant Juvenile Breast
Fibroadenoma in a Girl with Turner’s Syndrome |
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V. Calcaterra, D.R. Coscia,
A. Sgarella, B. Burroni, M. Podetta, A. Andorno, A. Ferrari and D. Larizza,
Pavia, Italy |
281 |
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CALENDAR |
285 |