Search Results - "Dörr, G"

Prevalence, Incidence and Risk Factors for Donor‐Specific Anti‐HLA Antibodies in Maintenance Liver Transplant Patients by Del Bello, A., Congy‐Jolivet, N., Muscari, F., Lavayssière, L., Esposito, L., Cardeau‐Desangles, I., Guitard, J., Dörr, G., Suc, B., Duffas, J. P., Alric, L., Bureau, C., Danjoux, M., Guilbeau‐Frugier, C., Blancher, A., Rostaing, L., Kamar, N.

“…Although large retrospective studies have identified the presence of donor‐specific antibodies (DSAs) to be a risk factor for rejection and impaired survival…”
Get full text

Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey by Raue, Friedhelm, Pichl, Josef, Dörr, Helmuth-G., Schnabel, Dirk, Heidemann, Peter, Hammersen, Gerhard, Jaursch-Hancke, Cornelia, Santen, Reinhard, Schöfl, Christof, Wabitsch, Martin, Haag, Christine, Schulze, Egbert, Frank-Raue, Karin

“…Summary Objective  Autosomal dominant hypocalcaemia or hypoparathyroidism is caused by activating mutations of the calcium‐sensing receptor (CaSR). Treatment…”
Get full text

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…”
Get full text

Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency by Dörr, Helmuth G, Hess, Johannes, Penger, Theresa, Marx, Michaela, Oppelt, Patricia

“…The most common form of congenital adrenal hyperplasia is 21-hydroxylase deficiency (CAH). Both men and women with classic CAH have lower fertility rates than…”
Get full text

Quality of Survival and Growth in Children and Young Adults in the PNET4 European Controlled Trial of Hyperfractionated Versus Conventional Radiation Therapy for Standard-Risk Medulloblastoma by Kennedy, Colin, MBBS, MD, Bull, Kim, PhD, Chevignard, Mathilde, MD, Culliford, David, MSc, Dörr, Helmuth G., MD, Doz, François, MD, Kortmann, Rolf-Dieter, MD, Lannering, Birgitta, MD, Massimino, Maura, MD, Navajas Gutiérrez, Aurora, MD, Rutkowski, Stefan, MD, Spoudeas, Helen A., MD, Calaminus, Gabriele, MD

“…Purpose To compare quality of survival in “standard-risk” medulloblastoma after hyperfractionated radiation therapy of the central nervous system with that…”
Get full text

Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency by Dörr, Helmuth G., Penger, Theresa, Albrecht, Andrea, Marx, Michaela, Völkl, Thomas M. K.

“…Classic congenital adrenal hyperplasia (CAH) secondary to 21-hydroxylase deficiency is characterized by increased prenatal adrenal androgen secretion. There…”
Get full text

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany by Dörr, Helmuth G, Wollmann, Hartmut A, Hauffa, Berthold P, Woelfle, Joachim

“…Adrenal crises in children with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (CAH) are life-threatening and have the potential to…”
Get full text

Impact of Early Blood Transfusion After Kidney Transplantation on the Incidence of Donor-Specific Anti-LA Antibodies by Ferrandiz, I., Congy-Jolivet, N., Del Bello, A., Debiol, B., Trébern-Launay, K., Esposito, L., Milongo, D., Dörr, G., Rostaing, L., Kamar, N.

Get full text

Adrenarche and pubarche in girls with turner syndrome during growth-promoting therapy with human growth hormone by Dörr, Helmuth G, Penger, Theresa, Marx, Michaela, Rauh, Manfred, Oppelt, Patricia G, Völkl, Thomas K M

“…Data on adrenarche and pubarche in girls with Turner syndrome (TS) are inconsistent in the literature. The cohort consisted of 94 girls and young women with TS…”
Get full text

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…”
Get more information

Simultaneously reduced gene expression of cortisol-activating and cortisol-inactivating enzymes in placentas of small-for-gestational-age neonates by Struwe, Ellen, MD, Berzl, Gabriele M., MD, Schild, Ralf L., MD, Beckmann, Matthias W., MD, Dörr, Helmuth G., MD, Rascher, Wolfgang, MD, Dötsch, Jörg, MD

“…Objective The enzyme 11β-hydroxysteroid dehydrogenase type 2 (11β-HSD2) converts cortisol into cortisone. Reduced placental activity of 11β-HSD2 in…”
Get full text

Intrauterine growth restriction (IUGR) is associated with increased leptin synthesis and binding capability in neonates by Tzschoppe, Anja, Struwe, Ellen, Rascher, Wolfgang, Dörr, Helmuth G., Schild, Ralf L., Goecke, Tamme W., Beckmann, Matthias W., Hofner, Benjamin, Kratzsch, Jürgen, Dötsch, Jörg

“…Summary Objective  Animal studies suggest pathological foetal programming of hypothalamic circuits regulating food intake in the setting of leptin deficiency…”
Get full text

Altered 24-Hour Blood Pressure Profiles in Children and Adolescents with Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency by Völkl, Thomas M. K., Simm, Diemud, Dötsch, Jörg, Rascher, Wolfgang, Dörr, Helmuth G.

“…Objective: Children and adolescents with classical congenital adrenal hyperplasia have been shown to be at risk for obesity associated with higher insulin and…”
Get full text

Stability of salivary steroids: the influences of storage, food and dental care by Gröschl, Michael, Wagner, Roland, Rauh, Manfred, Dörr, Helmut G

“…We studied influences of dental care, food and storage on the reproducibility of salivary steroid levels. Cortisol (F), 17OH-progesterone (17OHP) and…”
Get full text

Klinefelter syndrome and mediastinal germ cell tumors by Völkl, Thomas M.K., Langer, Thorsten, Aigner, Thomas, Greess, Holger, Beck, Jörn D., Rauch, Anita M., Dörr, Helmuth G.

“…Precocious puberty is not a typical manifestation of patients with Klinefelter syndrome (KS). However, there is an increased incidence of mediastinal germ cell…”
Get full text

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)…”
Get full text

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…”
Get more information

Impact of Early Blood Transfusion After Kidney Transplantation on the Incidence of Donor‐Specific Anti‐HLA Antibodies by Ferrandiz, I., Congy‐Jolivet, N., Del Bello, A., Debiol, B., Trébern‐Launay, K., Esposito, L., Milongo, D., Dörr, G., Rostaing, L., Kamar, N.

“…Little is known about the impact of posttransplant blood transfusion on the sensitization of anti‐HLA antibodies and the formation of donor‐specific antibodies…”
Get full text

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…”
Get full text

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…”
Get full text