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  1. Article

    Longitudinal study of 8 plasma mineralocorticoids(MC), glucocorticoids(GC) and progestins in premature infants (PI) at birth and during the neonatal period

    To evaluate fetoplacental and adrenocortical functions of the PI at birth and during postnatal adaptation, plasma aldosterone(Aldo), corticosterone(B), 11-deoxycorticosterone(DOC), progesterone(P), 17-hydroxyp...

    W G Sippell, H G Dörr, H T Versmold, F Bidlingmaier, D Knorr in Pediatric Research (1981)

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    Article

    Pseudohypoaldosteronism in a child with Down syndrome. Long-term management of salt loss by ion exchange resin administration

    At 4 weeks of age, an infant with Down syndrome developed severe dehydration and salt loss with the typical features of pseudohypoaldosteronism (PHA). Plasma renin activity, 11-deoxycorticosterone, corticoster...

    H. Saule, H. G. Dörr, W. G. Sippell in European Journal of Pediatrics (1984)

  3. Article

    EVIDENCE FOR A NATURALLY OCCURING MINERALOCORTICOIDANTAGONIST IN CONGENITAL ADRENAL HYPERPLASIA (CAH)

    The existence of a salt-excreting factor in CAH due to a 21-hydroxylase defect has been postulated for many years.However extensive investigations sofar were unable to isolate such a factor.Our demonstration o...

    U Kuhnle, H G Dörr, F Bidlingmaier, D Knorr, S Ulick in Pediatric Research (1984)

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  4. Article

    Etomidate (E): a potent inhibitor of adrenocortical 11 β-hydroxylase activity

    Increased mortality with long-term E infusions in intensive care patients has been reported and evidence is accumulating that E causes reversible adrenocortical suppression with decreased serum cortisol levels...

    H G Dörr, U Kuhnle, F Bidlingmaier, D Knorr in Pediatric Research (1984)

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  5. Article

    SMALL FOR GESTATIONAL AGE (SGA) INFANTS: PLASMA MINERALOCORTICOIDS, GLUCOCORTICOIDS AND PR0GESTINS AT BIRTH AND DURING THE NEONATAL PERIOD

    The small adrenal cortex of SGA infants may play a role in the pathogenesis of their frequent postnatal problems. We therefore evaluated adrenocortical function of SGA infants at birth and during postnatal ada...

    H G Dörr, H T Versmold, W G Sippell, F Bidlingmaier, D Knorr in Pediatric Research (1985)

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  6. Article

    PITFALLS OF PRENATAL TREATMENT OF CONGENITAL ADRENAL HYPERPLASIA (CAH) DUE TO 21-HYDROXYLASE DEFICIENCY

    It has been reported that prenatal dexamethasone (DEX) treatment of women carrying female CAH fetuses suppresses fetal adrenal function and prevents virilization of external genitalia. In 2 CAH families, the m...

    H G Dörr, W G Sippell, D Haack, F Bidlingmaier, D Knorr in Pediatric Research (1986)

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    Article

    Postnatal course of plasma levels of adrenocortical steroids in premature infants with and without NaCl supplementation

    To assess the adrenocortical response of premature infants to alterations in sodium balance, the postnatal course of plasma progesterone, 11-deoxycorticosterone, corticosternoe, aldosterone, 17-hydroxyprogeste...

    E. Sulyok, H. G. Dörr, T. Ertl, Gy. Gyódi in European Journal of Pediatrics (1988)

  8. No Access

    Chapter

    Erkrankungen der endokrinen Drüsen

    Der hypophysäre Minderwuchs ist durch eine verminderte Sekretion von Wachstumshormon (GH = Growth Hormone; STH = somatotropes Hormon = Somatropin) bedingt. Die primäre Störung kann in der Hypophyse selbst, im ...

    M. B. Ranke, H.-G. Dörr, G.-A. von Harnack… in Therapie der Krankheiten des Kindesalters (1991)

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    Chapter and Conference Paper

    Neurogene Blase bei Meningomyelozele — Bestandsaufnahme bei 121 Patienten und Therapiekonzept

    Das Wissen um die neurogene Blase und ihre Folgeprobleme hat sich vor allem dank urodynamischer Untersuchungen in den letzten Jahren erweitert und vertieft. Konservative Therapiekonzepte wurden entsprechend we...

    E. Strehl, R. Trollmann, G. Schott, S. Drexler, H. G. Dörr in Aktuelle Neuropädiatrie 1991 (1992)

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    Chapter and Conference Paper

    Neuere Aspekte der Behandlung und psychosozialen Betreuung von jungen Mädchen mit Ullrich-Turner-Syndrom

    Neben altersabhängigen Auffälligkeiten im äußeren Erscheinungsbild und verschiedenen Veränderungen innerer Organe sind der Kleinwuchs und die Gonadendysgenesie Hauptmerkmale des Ullrich-Turner-Syndroms (UTS) (...

    H. G. Dörr in Gynäkologie und Geburtshilfe 1992 (1993)

  11. Article

    PRENATAL TREATMENT OF CONGENITAL ADRENAL HYPERPLASIA (CAH) DUE TO 21-HYDROXYLASE DEFICIENCY: EUROPEAN EXPERIENCE IN 223 PREGNANCIES AT RISK

    In the aim to prevent the in utero virilization of CAH affected females a prenatal treatment (Rx) has first been attempted by David and Forest in 1979; later these authors reported their first results and propose...

    M G Forest, H G Dörr in Pediatric Research (1993)

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    Chapter

    Erkrankungen der endokrinen Drüsen

    Der hypophysäre Minderwuchs ist durch eine verminderte Sekretion von Wachstumshormon (GH = „growth hormone“; STH = somatotropes Hormon = Somatotroprin) bedingt. Die primäre Störung kann in der Hypophyse selbst...

    M. B. Ranke, H.-G. Dörr, G.-A. von Harnack… in Therapie der Krankheiten des Kindesalters (1994)

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    Article

    Endocrine disorders in septo-optic dysplasia (De Morsier syndrome) — evaluation and follow up of 18 patients

    Septo-optic dysplasia (SOD) is characterized by hypoplasia of the optic nerve, various types of forebrain defects and hormonal deficiencies. We have studied the clinical and endocrinological characteristics of...

    S. Willnow, W. Kiess, O. Butenandt, H. G. Dörr, A. Enders… in European Journal of Pediatrics (1996)

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    Article

    Anthropomorphic measurements of patients with myelomeningocele

    R. Trollmann, H. G. Dörr in European Journal of Pediatrics (1996)

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    Article

    Value of direct measurement of active renin concentrations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

    In congenital adrenal hyperplasia (CAR) due to 21-hydroxylase deficiency, measurement of plasma renin activity (PRA) has been the method of choice in diagnosing salt loss and in monitoring adequacy of mineralo...

    C. Krüger, K. Höper, R. Weissörtel, J. Hensen, H. G. Dörr in European Journal of Pediatrics (1996)

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    Article

    Neonatal diabetes and intra-uterine growth retardatihon

    C. Krüger, H. G. Dörr, K. E. von Mühlendahl… in European Journal of Pediatrics (1996)

  17. No Access

    Article

    Sekundäre Amenorrhö als erstes Symptom eines suprasellären Germinoms

    A. Koch, B. Zimmermann, D. Wenzel, H. G. Dörr in Monatsschrift Kinderheilkunde (1997)

  18. No Access

    Article

    Diagnostik des Williams-Beuren-Syndroms

    Anita Rauch, U. Trautmann, H. Singer, B. Kevekordes… in Monatsschrift Kinderheilkunde (1997)

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    Article

    Wachstum von Kindern in Remission nach Medulloblastomtherapie Analyse der 2-Jahres-Daten unter Therapie mit Wachstumshormon*,**

    U. Walden, A. Koch, J. D. Beck, H. G. Dörr in Monatsschrift Kinderheilkunde (1998)

  20. No Access

    Article

    Arm span, serum IGF-1 and IGFBP-3 levels as screening parameters for the diagnosis of growth hormone deficiency in patients with myelomeningocele – preliminary data

    Short stature is a common problem in patients with myelomeningocele (MMC) and hydrocephalus. We evaluated auxological and laboratory parameters to differentiate short stature due to neurological defect from s...

    R. Trollmann, E. Strehl, D. Wenzel, H. G. Dörr in European Journal of Pediatrics (1998)

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