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Kinderkrankenschwester : Organ Der Sektion Kinderkrankenpflege
|
August 23, 2014
[Autoimmune thyroiditis in childhood]
Susanne Fricke-Otto
Frontiers in Pediatrics
|
January 22, 2024
Case report: Life threatening hyponatremia in infants with urinary tract infections: two cases of type III pseudohypoaldosteronism and review of the literature
Cécile Carl, Lars Dinkelbach, Julia Mohr, et al.
Hormone Research
|
February 4, 2009
Height gains in response to growth hormone treatment to final height are similar in patients with SHOX deficiency and Turner syndrome
Werner F Blum, Dachuang Cao, Volker Hesse, et al.
International Journal of Neonatal Screening
|
March 6, 2021
Guideline Adherence and Registry Recruitment of Congenital Primary Hypothyroidism: Data from the German Registry for Congenital Hypothyroidism (HypoDok)
Julia Thomann, Sascha R Tittel, Egbert Voss, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
Twenty years of newborn screening for congenital adrenal hyperplasia and congenital primary hypothyroidism - experiences from the DGKED/AQUAPE study group for quality improvement in Germany
Johanna Hammersen, Markus Bettendorf, Walter Bonfig, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 10, 2004
SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity
Gerhard Binder, Alexandra Renz, Alicia Martinez, et al.
EMBO Molecular Medicine
|
November 19, 2016
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency
Antonino Montalbano, Lonny Juergensen, Ralph Roeth, et al.
Hormone Research in Paediatrics
|
October 27, 2017
Sodium Chloride Supplementation Is Not Routinely Performed in the Majority of German and Austrian Infants with Classic Salt-Wasting Congenital Adrenal Hyperplasia and Has No Effect on Linear Growth and Hydrocortisone or Fludrocortisone Dose
Walter Bonfig, Friedhelm Roehl, Stefan Riedl, et al.
Journal of Perinatal Medicine
|
February 14, 2019
Identification of growth patterns of preterm and small-for-gestational age children from birth to 4 years - do they catch up?
Dirk Manfred Olbertz, Rebekka Mumm, Ursula Wittwer-Backofen, et al.
Frontiers in Pediatrics
|
May 22, 2019
Quality of Life of Short-Statured Children Born Small for Gestational Age or Idiopathic Growth Hormone Deficiency Within 1 Year of Growth Hormone Treatment
Julia Quitmann, Janika Bloemeke, Neuza Silva, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Kinderkrankenschwester : Organ Der Sektion Kinderkrankenpflege
|
August 23, 2014
[Autoimmune thyroiditis in childhood]
Susanne Fricke-Otto
Frontiers in Pediatrics
|
January 22, 2024
Case report: Life threatening hyponatremia in infants with urinary tract infections: two cases of type III pseudohypoaldosteronism and review of the literature
Cécile Carl, Lars Dinkelbach, Julia Mohr, et al.
Hormone Research
|
February 4, 2009
Height gains in response to growth hormone treatment to final height are similar in patients with SHOX deficiency and Turner syndrome
Werner F Blum, Dachuang Cao, Volker Hesse, et al.
International Journal of Neonatal Screening
|
March 6, 2021
Guideline Adherence and Registry Recruitment of Congenital Primary Hypothyroidism: Data from the German Registry for Congenital Hypothyroidism (HypoDok)
Julia Thomann, Sascha R Tittel, Egbert Voss, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
Twenty years of newborn screening for congenital adrenal hyperplasia and congenital primary hypothyroidism - experiences from the DGKED/AQUAPE study group for quality improvement in Germany
Johanna Hammersen, Markus Bettendorf, Walter Bonfig, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 10, 2004
SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity
Gerhard Binder, Alexandra Renz, Alicia Martinez, et al.
EMBO Molecular Medicine
|
November 19, 2016
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency
Antonino Montalbano, Lonny Juergensen, Ralph Roeth, et al.
Hormone Research in Paediatrics
|
October 27, 2017
Sodium Chloride Supplementation Is Not Routinely Performed in the Majority of German and Austrian Infants with Classic Salt-Wasting Congenital Adrenal Hyperplasia and Has No Effect on Linear Growth and Hydrocortisone or Fludrocortisone Dose
Walter Bonfig, Friedhelm Roehl, Stefan Riedl, et al.
Journal of Perinatal Medicine
|
February 14, 2019
Identification of growth patterns of preterm and small-for-gestational age children from birth to 4 years - do they catch up?
Dirk Manfred Olbertz, Rebekka Mumm, Ursula Wittwer-Backofen, et al.
Frontiers in Pediatrics
|
May 22, 2019
Quality of Life of Short-Statured Children Born Small for Gestational Age or Idiopathic Growth Hormone Deficiency Within 1 Year of Growth Hormone Treatment
Julia Quitmann, Janika Bloemeke, Neuza Silva, et al.
Page
of 2