Search Results - "Dörr, H."

First-year predictors of health-related quality of life changes in short-statured children treated with human growth hormone by Quitmann, J., Bloemeke, J., Dörr, H.-G., Bullinger, M., Witt, S., Silva, N.

“…Purpose Little attention has been directed towards examining the impact of predictors on change in health-related quality of life (HRQOL) within the course of…”
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Rapid Prediction of Hematologic Acute Radiation Syndrome in Radiation Injury Patients Using Peripheral Blood Cell Counts by Port, M., Pieper, B., Knie, T., Dörr, H., Ganser, A., Graessle, D., Meineke, V., Abend, M.

“…Rapid clinical triage of radiation injury patients is essential for determining appropriate diagnostic and therapeutic interventions. We examined the utility…”
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Correlation of Radiation Dose Estimates by DIC with the METREPOL Hematological Classes of Disease Severity by Port, M., Pieper, B., Dörr, H. D., Hübsch, A., Majewski, M., Abend, M.

“…The degree of severity of hematologic acute radiation syndrome (HARS) may vary across the range of radiation doses, such that dose alone may be a less reliable…”
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Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase-Deficiency: 13 Years of Neonatal Screening and Follow-up in Bavaria by Odenwald, B, Dörr, H-G, Bonfig, W, Schmidt, H, Fingerhut, R, Wildner, M, Nennstiel-Ratzel, U

“…21-Hydroxylase deficient (21-OHD) classic congenital adrenal hyperplasia (CAH) is a potentially lethal inherited endocrine disorder. It is included in many…”
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Using Clinical Signs and Symptoms for Medical Management of Radiation Casualties – 2015 NATO Exercise by Dörr, H., Abend, M., Blakely, W. F., Bolduc, D. L., Boozer, D., Costeira, T., Dant, T., De Amicis, A., De Sanctis, S., Dondey, M., Drouet, M., Entine, F., Francois, S., Gagna, G., Guitard, N., Hérodin, F., Hoefer, M., Lamkowski, A., La Sala, G., Lista, F., Loiacono, P., Majewski, M., Martigne, P., Métivier, D., Michel, X., Pateux, J., Pejchal, J., Reeves, G., Riccobono, D., Sinkorova, Z., Soyez, L., Stricklin, D., Tichy, A., Valente, M., Woodruff Jr, C. R., Zarybnicka, L., Port, M.

“…The utility of early-phase (≤5 days) radiation-induced clinical signs and symptoms (e.g., vomiting, diarrhea, erythema and changes in blood cell counts) was…”
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LIQUID‐BIOPSY BASED GENOTYPING OF PRIMARY CENTRAL NERVOUS SYSTEM LYMPHOMA (PCNSL) by Heger, J.‐M., Gödel, P., Balke‐Want, H., Altmüller, J., Mattlener, J., Dörr, H., Weiss, J., Sieg, N., Kutsch, N., Reinhardt, H. C., Borchmann, P., von Tresckow, B., Borchmann, S.

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No Correlation between Androgen Receptor CAG and GGN Repeat Length and the Degree of Genital Virilization in Females with 21-Hydroxylase Deficiency by Welzel, M., Schwarz, H.-P., Hedderich, J., Dörr, H. G., Binder, G., Brämswig, J. H., Krude, H., Richter-Unruh, A., Niedziela, M., Gromoll, J., Krone, N., Riepe, F. G., Holterhus, P.-M.

“…Context: In 21-hydroxylase (CYP21A2) deficiency (21OHD), the level of in vitro enzymatic function allows for classification of mutation groups (null, A, B, C)…”
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Naltrexone as a diagnostic tool to distinguish between hyperandrogenemic and hypothalamic ovarian failure in females with congenital adrenal hyperplasia due to 21-hydroxylase-deficiency (CAH) by Böttcher, B, Dörr, H.G, Wildt, L

“…Abstract Objective Hypothalamic ovarian failure can be considered as a differential diagnosis in women suffering from CAH and amenorrhea. Naltrexone can be…”
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Differences in gene expression dependent on sampling site in placental tissue of fetuses with intrauterine growth restriction by Tzschoppe, A.A, Struwe, E, Dörr, H.G, Goecke, T.W, Beckmann, M.W, Schild, R.L, Dötsch, J

“…Abstract Objective The human placenta as part of the feto-placental unit may influence fetal endocrine systems and may therefore represent a very important…”
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Größenwachstum und Knochengesundheit bei Erkrankungen der Wachstumsfuge und des Knochens: Möglichkeiten und Grenzen einer GH-Therapie by Wölfle, J., Bettendorf, M., Bechtold-Dalla Pozza, S., Binder, G., Grasemann, C., Reinehr, T., Semler, O., Dörr, H.-G.

“…Zusammenfassung Hintergrund Genetische, parakrine und endokrine Faktoren beeinflussen das Größenwachstum und die Knochenmineralisation. Fragestellung Wie sind…”
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Experts' Opinion on the Prenatal Therapy of Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency - Guideline of DGKED in cooperation with DGGG (S1-Level, AWMF Registry No. 174/013, July 2015) by Dörr, H G, Binder, G, Reisch, N, Gembruch, U, Oppelt, P G, Wieacker, P, Kratzsch, J

“…This guideline of the German Society of Pediatric Endocrinology and Diabetology (DGKED) is designed to be experts' opinion on the current concept of prenatal…”
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Glukokortikoide bei nichtendokrinen Erkrankungen, bei Kortisolmangel und bei endogenem Exzess – der Einfluss therapeutischer Strategien auf das kindliche Wachstum by Hauffa, B. P., Binder, G., Bonfig, W., Bettendorf, M., Dörr, H.-G.

“…Zusammenfassung Hintergrund Nebennierenrindenhormone können das Wachstum von Kindern und Jugendlichen beeinflussen. Fragestellung Wie beeinflussen chronische…”
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The placental mTOR-pathway: correlation with early growth trajectories following intrauterine growth restriction? by Fahlbusch, F B, Hartner, A, Menendez-Castro, C, Nögel, S C, Marek, I, Beckmann, M W, Schleussner, E, Ruebner, M, Huebner, H, Dörr, H-G, Schild, R L, Dötsch, J, Rascher, W

“…Idiopathic intrauterine growth restriction (IUGR) is a result of impaired placental nutrient supply. Newborns with IUGR exhibiting postnatal catch-up growth…”
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Detection of Herpes Simplex Virus DNA by Real-Time PCR by Kessler, Harald H., Mühlbauer, Gerhard, Rinner, Beate, Stelzl, Evelyn, Berger, Annemarie, Dörr, Hans-Wilhelm, Santner, Brigitte, Marth, Egon, Rabenau, Holger

“…Article Usage Stats Services JCM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutations by HOLTERHUS, P. M, WERNER, R, HOPPE, U, BASSLER, J, KORSCH, E, RANKE, M. B, DÖRR, H. G, HIORT, O

“…Androgen insensitivity syndrome (AIS) is characterized by deficient or absent virilization in 46,XY individuals despite normal or even elevated androgen…”
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Long-term Surveillance of Children with Congenital Hypothyroidism: Data from the German Registry for Congenital Hypothyroidism (AQUAPE "Hypo Dok") by Ellerbroek, V L, Bonfig, W, Dörr, H-G, Bettendorf, M, Hauffa, B, Fricke-Otto, S, Rohrer, T, Reschke, F, Schönau, E, Schwab, K O, Kapelari, K, Röhl, F-W, Mohnike, K, Holl, R W

“…The German study group for quality assurance in pediatric endocrinology and the University of Ulm have established a software ("Hypo Dok") for the…”
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The effects of art therapy on anxiety, depression, and quality of life in adults with cancer: a systematic literature review by Bosman, J. T., Bood, Z. M., Scherer-Rath, M., Dörr, H., Christophe, N., Sprangers, M. A. G., van Laarhoven, H. W. M.

“…Purpose While there is increasing evidence for the effectiveness of psychosocial support programs for cancer patients, little attention has been paid to…”
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Late endocrine sequelae after radiotherapy of pediatric brain tumors are independent of tumor location by Rohrer, T. R., Beck, J. D., Grabenbauer, G. G., Fahlbusch, R., Buchfelder, M., Dörr, H. G.

“…Introduction : Irradiation of brain tumors (BT) in children can lead to the loss of pituitary function, predominantly manifesting as deficiencies in GH and…”
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Thyroid function in paediatric and young adult patients after sarcoma therapy: a report from the Late Effects Surveillance System by Paulides, M., Dörr, H. G., Stöhr, W., Bielack, S., Koscielniak, E., Klingebiel, T., Jürgens, H., Bölling, T., Willich, N., Sauer, R., Langer, T., Beck, J. D.

“…Summary Objective  The role of chemotherapy in thyroid sequelae after cancer treatment has not been studied systematically, especially in sarcoma patients. The…”
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Infantile hypophosphatasia due to a new compound heterozygous TNSALP mutation - functional evidence for a hydrophobic side-chain? by Utsch, B, Brun-Heath, I, Staatz, G, Gravou-Apostolatou, C, Karle, S, Jacobs, U, Ludwig, M, Zenker, M, Dörr, H-G, Rascher, W, Mornet, E, Dötsch, J

“…Infantile hypophosphatasia (IH) is an inherited disorder characterized by defective bone mineralization and a deficiency of alkaline phosphatase activity. The…”
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