Search Results - "Vollbach, Heike"

Serum IGF1 and linear growth in children with congenital leptin deficiency before and after leptin substitution by Beghini, Marianna, Brandt, Stephanie, Körber, Ingrid, Kohlsdorf, Katja, Vollbach, Heike, Lennerz, Belinda, Denzer, Christian, Shalitin, Shlomit, Santini, Ferruccio, Blum, Werner F., von Schnurbein, Julia, Wabitsch, Martin

“…Background Evidence from in vitro and rodent studies suggests that leptin, a key signal of long-term energy reserves, promotes IGF1 synthesis and linear…”
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Treatment of Hypothalamic Obesity with Dextroamphetamine: A Case Series by Denzer, Christian, Denzer, Friederike, Lennerz, Belinda S., Vollbach, Heike, Lustig, Robert H., Wabitsch, Martin

“…Background: A limited number of published case reports suggest a positive effect of dextroamphetamine, an adrenergic agonist affecting both the central nervous…”
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Case Report: Extended Clinical Spectrum of the Neonatal Diabetes With Congenital Hypothyroidism Syndrome by Splittstoesser, Vera, Vollbach, Heike, Plamper, Michaela, Garbe, Werner, De Franco, Elisa, Houghton, Jayne A L, Dueker, Gesche, Ganschow, Rainer, Gohlke, Bettina, Schreiner, Felix

“…Neonatal diabetes with congenital hypothyroidism (NDH) syndrome is a rare condition caused by homozygous or compound heterozygous mutations in the…”
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Genomic Basis of Aromatase Excess Syndrome: Recombination- and Replication-Mediated Rearrangements Leading to CYP19A1 Overexpression by Fukami, Maki, Tsuchiya, Takayoshi, Vollbach, Heike, Brown, Kristy A, Abe, Shuji, Ohtsu, Shigeyuki, Wabitsch, Martin, Burger, Henry, Simpson, Evan R, Umezawa, Akihiro, Shihara, Daizou, Nakabayashi, Kazuhiko, Bulun, Serdar E, Shozu, Makio, Ogata, Tsutomu

“…Context: Genomic rearrangements at 15q21 have been shown to cause overexpression of CYP19A1 and resultant aromatase excess syndrome (AEXS). However, mutation…”
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Innovative medizinische Betreuungskonzepte für Jugendliche mit extremer Adipositas by Wabitsch, Martin, v. Schnurbein, Julia, Vollbach, Heike, Lennerz, Belinda, Weyhreter, Helmut, Wiegand, Susanna, Kiess, Wieland, Hebebrand, Johannes, Brandt, Stephanie

“…Zusammenfassung Für Jugendliche mit extremer Adipositas gibt es bislang kein überzeugendes, wissenschaftsbasiertes Behandlungs- und Betreuungskonzept, weder in…”
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Phenylbutyrate Treatment in a Boy with MCT8 Deficiency: Improvement of Thyroid Function Tests and Possible Livertoxicity by Schreiner, Felix, Vollbach, Heike, Sonntag, Niklas, Schempp, Vera, Gohlke, Bettina, Friese, Johannes, Woelfle, Joachim, Braun, Doreen, Schweizer, Ulrich

“…Monocarboxylate transporter 8 (MCT8) deficiency is a rare X-chromosomal inherited disease leading to severe cognitive impairment, muscular hypotonia and…”
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Sleep and glycemic control in adolescents with type 1 diabetes by von Schnurbein, Julia, Boettcher, Claudia, Brandt, Stephanie, Karges, Beate, Dunstheimer, Desiree, Galler, Angela, Denzer, Christian, Denzer, Friederike, Vollbach, Heike, Wabitsch, Martin, Roenneberg, Till, Vetter, Celine

“…Background Increasing evidence link sleep curtailment and circadian misalignment with adverse metabolic outcome. Adolescents might be most affected, given…”
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Early childhood BMI trajectories in monogenic obesity due to leptin, leptin receptor, and melanocortin 4 receptor deficiency by Kohlsdorf, Katja, Nunziata, Adriana, Funcke, Jan-Bernd, Brandt, Stephanie, von Schnurbein, Julia, Vollbach, Heike, Lennerz, Belinda, Fritsch, Maria, Greber-Platzer, Susanne, Fröhlich-Reiterer, Elke, Luedeke, Manuel, Borck, Guntram, Debatin, Klaus-Michael, Fischer-Posovszky, Pamela, Wabitsch, Martin

“…Objective: To evaluate whether early childhood body mass index (BMI) is an appropriate indicator for monogenic obesity. Methods: A cohort of n  = 21 children…”
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Methylphenidate in children with monogenic obesity due to LEPR or MC4R deficiency improves feeling of satiety and reduces BMI‐SDS—A case series by Brandt, Stephanie, Schnurbein, Julia, Lennerz, Belinda, Kohlsdorf, Katja, Vollbach, Heike, Denzer, Christian, Bode, Harald, Hebebrand, Johannes, Wabitsch, Martin

“…Summary Background The clinical phenotype of patients with monogenic obesity due to mutations in the leptin receptor (LEPR) or melanocortin 4 receptor (MC4R)…”
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Choice of basal insulin therapy is associated with weight and height development in type 1 diabetes: A multicenter analysis from the German/Austrian DPV registry in 10338 children and adolescents by Vollbach, Heike, Auzanneau, Marie, Reinehr, Thomas, Wiegand, Susanna, Karl‐Otfried Schwab, Oeverink, Rudolf, Elke Froehlich‐Reiterer, Woelfle, Joachim, De Beaufort, Carine, Kapellen, Thomas, Gohlke, Bettina, Holl, Reinhard W

“…BackgroundAvailable basal insulin regimes differ in pharmacokinetic profiles, which may be related to subsequent changes in anthropometry in patients with type…”
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Choice of basal insulin therapy is associated with weight and height development in type 1 diabetes: A multicenter analysis from the German/Austrian DPV registry in 10 338 children and adolescents by Vollbach, Heike, Auzanneau, Marie, Reinehr, Thomas, Wiegand, Susanna, Schwab, Karl‐Otfried, Oeverink, Rudolf, Froehlich‐Reiterer, Elke, Woelfle, Joachim, De Beaufort, Carine, Kapellen, Thomas, Gohlke, Bettina, Holl, Reinhard W.

“…Background Available basal insulin regimes differ in pharmacokinetic profiles, which may be related to subsequent changes in anthropometry in patients with…”
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Sleep and glycemic control in adolescents with type 1 diabetes: von SCHNURBEIN et al by von Schnurbein, Julia, Boettcher, Claudia, Brandt, Stephanie, Karges, Beate, Dunstheimer, Desiree, Galler, Angela, Denzer, Christian, Denzer, Friederike, Vollbach, Heike, Wabitsch, Martin, Roenneberg, Till, Vetter, Celine

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APOA1 polymorphism influences risk for early-onset nonfamiliar AD by Vollbach, Heike, Heun, Reinhard, Morris, Chris M., Edwardson, Jim A., McKeith, Ian G., Jessen, Frank, Schulz, Anne, Maier, Wolfgang, Kölsch, Heike

“…Alterations in cholesterol homeostasis influence the risk for Alzheimer's disease (AD). Apolipoprotein A1 is the major apolipoprotein of the high‐density…”
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Frühkindlicher BMI-Verlauf bei monogener Adipositas by Kohlsdorf, Katja, Nunziata, Adriana, Funcke, Jan-Bernd, Brandt, Stephanie, von Schnurbein, Julia, Vollbach, Heike, Lennerz, Belinda, Fritsch, Maria, Greber-Platzer, Susanne, Fröhlich-Reiterer, Elke, Borck, Guntram, Fischer-Posovszky, Pamela, Wabitsch, Martin

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Innovative medical care concepts for adolescents with severe obesity by Wabitsch, Martin, V Schnurbein, Julia, Vollbach, Heike, Lennerz, Belinda, Weyhreter, Helmut, Wiegand, Susanna, Kiess, Wieland, Hebebrand, Johannes, Brandt, Stephanie

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Frühkindlicher BMI-Verlauf bei monogener Adipositas by Kohlsdorf, Katja, Nunziata, Adriana, Funcke, Jan-Bernd, Brandt, Stephanie, von Schnurbein, Julia, Vollbach, Heike, Lennerz, Belinda, Fritsch, Maria, Greber-Platzer, Susanne, Fröhlich-Reiterer, Elke, Borck, Guntram, Fischer-Posovszky, Pamela, Wabitsch, Martin

“…Zusammenfassung Hintergrund Monogene Adipositasformen haben eine geschätzte Prävalenz von 1–5 % in der Gruppe der extrem adipösen Patienten. Bereits im frühen…”
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Case Report: Extended Clinical Spectrum of the Neonatal Diabetes With Congenital Hypothyroidism Syndrome by Splittstoesser, Vera, Vollbach, Heike, Plamper, Michaela, Garbe, Werner, De Franco, Elisa, Houghton, Jayne A L, Dueker, Gesche, Ganschow, Rainer, Gohlke, Bettina, Schreiner, Felix

“…BackgroundNeonatal diabetes with congenital hypothyroidism (NDH) syndrome is a rare condition caused by homozygous or compound heterozygous mutations in the…”
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