Publications by authors named "Ralf Herrmann"

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Prenatal inflammation exacerbates hyperoxia-induced neonatal brain injury.
Meray Serdar, Kay-Anja Walther, Markus Gallert, Karina Kempe, Stefanie Obst, Ralf Herrmann

J Neuroinflammation· February 2025

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Proteomic and bioinformatic profiling of neutrophils in CLL reveals functional defects that predispose to bacterial infections.
Nirojah Subramaniam, Jenny Bottek, Stephanie Thiebes, Kristina Zec, Matthias Kudla, Ralf Herrmann

Blood Adv· March 2021

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Involvement of CXCL1/CXCR2 During Microglia Activation Following Inflammation-Sensitized Hypoxic-Ischemic Brain Injury in Neonatal Rats.
Meray Serdar, Karina Kempe, Ralf Herrmann, Daniel Picard, Marc Remke

Front Neurol· October 2020

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Are Simple Magnetic Resonance Imaging Biomarkers Predictive of Neurodevelopmental Outcome at Two Years in Very Preterm Infants?
Monia Vanessa Dewan, Ralf Herrmann, Bernd Schweiger, Selma Sirin, Hanna Müller

Neonatology· June 2020

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Plasma concentrations of osteocalcin are associated with the timing of pubertal progress in boys.
Michael M Schündeln, Lena Bäder, Cordula Kiewert, Ralf Herrmann, Dagmar Führer

J Pediatr Endocrinol Metab· February 2017

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Loss of Functional Osteoprotegerin: More Than a Skeletal Problem.
Corinna Grasemann, Nicole Unger, Matthias Hövel, Diana Arweiler-Harbeck, Ralf Herrmann

J Clin Endocrinol Metab· January 2017

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Fingolimod protects against neonatal white matter damage and long-term cognitive deficits caused by hyperoxia.
Meray Serdar, Josephine Herz, Karina Kempe, Katharina Lumpe, Barbara S Reinboth, Ralf Herrmann

Brain Behav Immun· February 2016

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Maternal vitamin D status in preeclampsia: seasonal changes are not influenced by placental gene expression of vitamin D metabolizing enzymes.
Carolin Lechtermann, Berthold P Hauffa, Ralf Herrmann, Michael M Schündeln, Alexandra Gellhaus

PLoS One· May 2015

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Effect of propofol in the immature rat brain on short- and long-term neurodevelopmental outcome.
Tanja Karen, Gerald W Schlager, Ivo Bendix, Marco Sifringer, Ralf Herrmann

PLoS One· January 2014

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Effects of RANK-ligand antibody (denosumab) treatment on bone turnover markers in a girl with juvenile Paget's disease.
Corinna Grasemann, Michael M Schündeln, Matthias Hövel, Bernd Schweiger, Christoph Bergmann, Ralf Herrmann

J Clin Endocrinol Metab· August 2013

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Parental diabetes: the Akita mouse as a model of the effects of maternal and paternal hyperglycemia in wildtype offspring.
Corinna Grasemann, Maureen J Devlin, Paulina A Rzeczkowska, Ralf Herrmann, Bernhard Horsthemke

PLoS One· June 2013

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ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies.
Sebahattin Cirak, Aileen Reghan Foley, Ralf Herrmann, Tobias Willer, Shu Yau

Brain· January 2013

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Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations.
Velina Guergueltcheva, Juliane S Müller, Marina Dusl, Jan Senderek, Anders Oldfors, Ralf Herrmann

J Neurol· May 2012

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Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect.
Jan Senderek, Juliane S Müller, Marina Dusl, Tim M Strom, Velina Guergueltcheva, Ralf Herrmann

Am J Hum Genet· February 2011

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Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy.
Sebahattin Cirak, Florian von Deimling, Shrikesh Sachdev, Wesley J Errington, Ralf Herrmann

Brain· July 2010

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Expression of SNURF-SNRPN upstream transcripts and epigenetic regulatory genes during human spermatogenesis.
Michaela Wawrzik, Andrej-Nikolai Spiess, Ralf Herrmann, Karin Buiting, Bernhard Horsthemke

Eur J Hum Genet· November 2009

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Caveolinopathy--new mutations and additional symptoms.
Ahmed Aboumousa, Jessica Hoogendijk, Richard Charlton, Rita Barresi, Ralf Herrmann

Neuromuscul Disord· July 2008

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Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome.
Jeroen van Reeuwijk, Prabhjit K Grewal, Mustafa A M Salih, Daniel Beltrán-Valero de Bernabé, Jenny M McLaughlan, Ralf Herrmann

Hum Genet· July 2007

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Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy.
Jan Senderek, Michael Krieger, Claudia Stendel, Carsten Bergmann, Markus Moser, Ralf Herrmann

Nat Genet· December 2005

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Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers.
Mariz Vainzof, Pascale Richard, Ralf Herrmann, Cecilia Jimenez-Mallebrera, Beril Talim

Neuromuscul Disord· October 2005

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125th ENMC International Workshop: Neuromuscular disorders in the Roma (Gypsy) population, 23-25 April 2004, Naarden, The Netherlands.
Luba Kalaydjieva, Hanns Lochmüller, Ivailo Tournev, Frank Baas, Judit Beres, Ralf Herrmann

Neuromuscul Disord· January 2005

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Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).
Christopher Meredith, Ralf Herrmann, Cheryl Parry, Khema Liyanage, Danielle E Dye

Am J Hum Genet· October 2004

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Phenotypic spectrum associated with mutations in the fukutin-related protein gene.
Eugenio Mercuri, Martin Brockington, Volker Straub, Susana Quijano-Roy, Yeliz Yuva, Ralf Herrmann

Ann Neurol· April 2003

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Deficiency of alpha-dystroglycan in muscle-eye-brain disease.
Hiroki Kano, Kazuhiro Kobayashi, Ralf Herrmann, Masaji Tachikawa, Hiroshi Manya

Biochem Biophys Res Commun· March 2002

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