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Results of search for 'au:"l'Allemand, D"', page 1 of 2
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Authors
Beyer, P
Biason-Lauber, A
Eiholzer, U
Grüters, A
Helge, H
Holl, R W
Krude, H
Köhler, B
L'Allemand, D
Morel, Y
Penhoat, A
Reinehr, T
Royer-Pokora, B
Saez, J M
Schlumpf, M
Schnabel, D
Schumacher, V
Schürnbrand, P
Weber, B
l'Allemand, D
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Topics
Adipose Tissue
Adolescent
Adrenal Cortex
Body Composition
Child
Child, Preschool
Female
Humans
Infant
Infant, Newborn
Male
Obesity
Prader-Willi Syndrome
Thyrotropin
administration & dosage
blood
drug therapy
epidemiology
genetics
metabolism
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English
French
German
Your search returned 28 results.
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1.
Growth hormone normalises height, prediction of final height and hand length in children with Prader-Willi syndrome after 4 years of therapy.
[electronic resource]
by
Eiholzer, U
l'Allemand, D
Producer:
20001130
In:
Hormone research
vol. 53
Online resources:
Available from publisher's website
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2.
Intra-adrenal regulation of androgen synthesis.
[electronic resource]
by
l'Allemand, D
Biason-Lauber, A
Producer:
20010607
In:
European journal of clinical investigation
vol. 30 Suppl 3
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3.
Is there growth hormone deficiency in prader-willi Syndrome? Six arguments to support the presence of hypothalamic growth hormone deficiency in Prader-Willi syndrome.
[electronic resource]
by
Eiholzer, U
Bachmann, S
l'Allemand, D
Producer:
20001011
In:
Hormone research
vol. 53 Suppl 3
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4.
Thyroid function and obesity in children and adolescents.
[electronic resource]
by
Stichel, H
l'Allemand, D
Grüters, A
Producer:
20010503
In:
Hormone research
vol. 54
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5.
Iodine-induced alterations of thyroid function in newborn infants after prenatal and perinatal exposure to povidone iodine.
[electronic resource]
by
l'Allemand, D
Grüters, A
Heidemann, P
Schürnbrand, P
Producer:
19830708
In:
The Journal of pediatrics
vol. 102
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6.
Iodine in contrast agents and skin disinfectants is the major cause for hypothyroidism in premature infants during intensive care.
[electronic resource]
by
l'Allemand, D
Grüters, A
Beyer, P
Weber, B
Producer:
19880527
In:
Hormone research
vol. 28
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7.
Early manifestations of Prader-Willi syndrome: influence of growth hormone.
[electronic resource]
by
Eiholzer, U
Schlumpf, M
Nordmann, Y
l'Allemand, D
Producer:
20020719
In:
Journal of pediatric endocrinology & metabolism : JPEM
vol. 14 Suppl 6
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8.
Is there a local IGF-system in human adrenocortical cells?
[electronic resource]
by
l'Allemand, D
Penhoat, A
Blum, W
Saez, J M
Producer:
19981104
In:
Molecular and cellular endocrinology
vol. 140
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9.
Incidence of iodine contamination in neonatal transient hyperthyrotropinemia.
[electronic resource]
by
Grüters, A
l'Allemand, D
Heidemann, P H
Schürnbrand, P
Producer:
19831220
In:
European journal of pediatrics
vol. 140
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10.
Cardiovascular risk factors improve during 3 years of growth hormone therapy in Prader-Willi syndrome.
[electronic resource]
by
l'Allemand, D
Eiholzer, U
Schlumpf, M
Steinert, H
Riesen, W
Producer:
20010531
In:
European journal of pediatrics
vol. 159
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11.
Ring Y chromosome: cytogenetic and molecular characterization.
[electronic resource]
by
Wegner, R D
Scherer, G
Pohlschmidt, M
L'Allemand, D
Gal, A
Producer:
19921202
In:
Clinical genetics
vol. 42
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12.
Germline Wilms tumor suppressor gene (WT1) mutation leading to isolated genital malformation without Wilms tumor or nephropathy.
[electronic resource]
by
Köhler, B
Schumacher, V
l'Allemand, D
Royer-Pokora, B
Grüters, A
Producer:
20010405
In:
The Journal of pediatrics
vol. 138
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13.
[Adrenal cortex function in children with bronchial asthma in fluticasone therapy].
[electronic resource]
by
Hoffmann-Streb, A
L'Allemand, D
Niggemann, B
Büttner, P
Wahn, U
Producer:
19930826
In:
Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde
vol. 141
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14.
How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency.
[electronic resource]
by
L'Allemand, D
Tardy, V
Grüters, A
Schnabel, D
Krude, H
Morel, Y
Producer:
20010202
In:
The Journal of clinical endocrinology and metabolism
vol. 85
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15.
Nonclassical adrenal hyperplasia due to 21-hydroxylase-deficiency: does genotyping predict the clinical manifestation?
[electronic resource]
by
l'Allemand, D
Keller, E
Hoeppner, W
Serban, A
Morel, Y
Grüters, A
Producer:
19970313
In:
Endocrine research
vol. 22
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16.
The use of L-T4 as liquid solution improves the practicability and individualized dosage in newborns and infants with congenital hypothyroidism.
[electronic resource]
by
von Heppe, J H
Krude, H
L'Allemand, D
Schnabel, D
Grüters, A
Producer:
20050329
In:
Journal of pediatric endocrinology & metabolism : JPEM
vol. 17
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17.
Aldosterone metabolism in rat renal tissue in vitro. Formation of lipid soluble metabolites.
[electronic resource]
by
l'Allemand, D
Siebe, H
Tsiakiras, D
Hoyer, G A
Vecsei, P
Hierholzer, K
Producer:
19880811
In:
Pflugers Archiv : European journal of physiology
vol. 411
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18.
[How to treat childhood obesity? Importance of primary prevention].
[electronic resource]
by
Farpour-Lambert, N J
Nydegger, A
Kriemler, S
L'Allemand, D
Puder, J J
Producer:
20080530
In:
Revue medicale suisse
vol. 4
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19.
Body composition abnormalities in children with Prader-Willi syndrome and long-term effects of growth hormone therapy.
[electronic resource]
by
Eiholzer, U
l'Allemand, D
van der Sluis, I
Steinert, H
Gasser, T
Ellis, K
Producer:
20001130
In:
Hormone research
vol. 53
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20.
Clinical, genetic and functional characteristics of three novel CYP17A1 mutations causing combined 17alpha-hydroxylase/17,20-lyase deficiency.
[electronic resource]
by
Rosa, S
Steigert, M
Lang-Muritano, M
l'Allemand, D
Schoenle, E J
Biason-Lauber, A
Producer:
20100524
In:
Hormone research in paediatrics
vol. 73
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