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Syndromic forms of congenital hyperinsulinism
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In: Hormone Research in Paediatrics, 2014, S. , ISSN 1663-2826, 10.1159/000356905

Universal newborn hearing screening : Definition of uniform parameters by the Association of German Hearing Screening Centers as a requirement for nationwide evaluation with valid results
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Klinisches Spektrum von Achondroplasie und Hypochondroplasie
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Sonometrie bei Achondroplasie
In: Achondroplasie und Hypochondroplasie - Diagnostik und Betreuung spezifischer Kleinwuchsformen: Diagnostik und Betreuung spezifischer Kleinwuchsformen - Berlin: ABW, Wissenschaftsverlag, 2013 . - 2013, S. 41-50

Medikamentöse Therapieoptionen bei Achondroplasie und Hypochondroplasie
In: Achondroplasie und Hypochondroplasie - Diagnostik und Betreuung spezifischer Kleinwuchsformen: Diagnostik und Betreuung spezifischer Kleinwuchsformen - Berlin: ABW, Wissenschaftsverlag, 2013 . - 2013, S. 155-160

Neugeborenenscreening auf angeborene Stoffwechsel- und Hormonstörungen in Deutschland
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Handlungsempfehlung nach der Leitlinie Pubertas praecox
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Achondroplasie und Hypochondroplasie - Diagnostik und Betreuung spezifischer Kleinwuchsformen
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Insulinome
In: Solide Tumoren im Kindesalter: Grundlagen - Diagnostik - Therapie ; mit 72 Tabellen ; inkl. DVD mit Tumoroperationen / hrsg. von Jörg Fuchs. Unter Mitarb. von Winfried Barthlen ...: Grundlagen - Diagnostik - Therapie ; mit 72 Tabellen ; inkl. DVD mit Tumoroperationen - Stuttgart: Schattauer, 2012 . - 2012, S. 283-286

Kongenitaler Hyperinsulinismus
In: Solide Tumoren im Kindesalter: Grundlagen - Diagnostik - Therapie ; mit 72 Tabellen ; inkl. DVD mit Tumoroperationen / hrsg. von Jörg Fuchs. Unter Mitarb. von Winfried Barthlen ...: Grundlagen - Diagnostik - Therapie ; mit 72 Tabellen ; inkl. DVD mit Tumoroperationen - Stuttgart: Schattauer, 2012 . - 2012, S. 288-293

Pädiatrie
In: PET/CT-Atlas , 2. Aufl. - Berlin : Springer ; Mohnike, Wolfgang *1949-* . - 2011, S. 845-892

Techniques in pediatric surgery: congenital hyperinsulinism
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Visualization of the focus in congenital hyperinsulinism by intraoperative sonography
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Glucose metabolism and neurological outcome in congenital hyperinsulinism
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Intraoperative Sonography: A Technique for Localizing Focal Forms of Congenital Hyperinsulinism in the Pancreas - Intraoperative Sonografie: eine Methode zur Lokalisation der fokalen Form des kongenitalen Hyperinsulinismus im Pankreas
In: Ultraschall in der Medizin - Stuttgart : Thieme, Bd. 32 (2011), Heft 1, S. 74-80

Endokrinologische Störungen
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Angeborene Knochenerkrankungen
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Techniques in pediatric surgery: congenital hyperinsulinism
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Congenital hyperinsulinism
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Planungsunterstützung für Pankreasoperationen bei Hyperinsulinismus von Kindern
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Cholesterin - zwischen Mangel und Überfluss - 20. Jahrestagung 2006 der Arbeitsgemeinschaft für Pädiatrische Stoffwechselstörungen (APS), Fulda
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Long-term non-surgical therapy of severe persistent congenital hyperinsulinism with glucagon
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Congenital hyperinsulinism: [18F]DOPA PET/CT scan of a focal lesion in the head of the pancreas
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Evaluation of (18F)Fluoro-L-DOPA positron emission tomography-computed tomography for surgery in focal congenital hyperinsulinism
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Metabolische Krisen im Kindesalter
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Diastrophe Dysplasie und Spondyloepiphysäre Dysplasie - Diagnostik, Betreuung und Langzeitkonsequenzen
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Diastrophe Dysplasie und Spondyloepiphysäre Dysplasie - Diagnostik, Betreuung und Langzeitkonsequenzen
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Congenital cataract, ataxia, external ophthalmoplegia and dysphagia in two siblings - a Marinesco-Sjögren-Like syndrome
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Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTC
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Distribution of sex chromosomes in dysgenetic gonads of mixed type
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Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTC
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Congenital cataract, ataxia, external ophthalmoplegia and dysphagia in two siblings - a Marinesco-Sjögren-Like syndrome
In: Neuropediatrics - Stuttgart [u.a.] : Thieme, Bd. 38 (2007), Heft 2, S. 88-90

Mikrosonographie der Schilddrüse im Kindesalter
In: München: Marseille, 2007, 64 S, Ill.

Nesidioblastose (angeborener Hyperinsulinismus)
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Proposal for a standardized protocol for 18F-DOPA-PET (PET/CT) in congenital hyperinsulinism
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Proposal for a standardized protocol for 18F-DOPA-PET (PET/CT) in congenital hyperinsulinism
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Das Klinefelter-Syndrom
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CranioNet - eine interdisziplinäre Strategie für das Kraniopharyngeom - CranioNet - an interdisciplinary strategy for craniopharyngioma
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Rationelle Diagnostik bei kindlichen Hypoglykämien
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Rationelle Diagnostik bei kindlichen Hypoglykämien
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Mutation typing in patients with medium chain AcylCoA dehydrogenase deficiency (MCADD) and PCR based mutation screening in SIDS victims
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Zur Geschichte des Phosphatdiabetes.
In:

Grundzüge der Therapie im Kindesalter.
In:

Insulin-like growth factor binding protein-2 at diagnosis of childhood acute lymphoblastic leukemia and the prediction of relapse risk.
In:

Novel and recurrent mutations in patients with androgen insensitivity syndromes.
In:

}... Growth hormone treatment in 35 prepubertal children with achondroplasia : a five-year dose- response trial.
In:

Proteus syndrome : successful therapy of severe migraine symptoms with low molecular weight heparin.
In:

Vorgeburtliches Wachstum, Schwangerschaftsdauer, Gewicht und Länge bei Geburt.
In:

Wachstum und Gewichtszunahme in den ersten Lebensjahren : Magdeburger Kohorte 1969-77.
In:

Serum MEPE-ASARM-peptides are elevated in X-linked rickets (HYP) : implications for phosphaturia and rickets.
In:

Tolerability of the Biken acellular pertussis vaccine in adults with or without previous vaccination against pertussis in childhood.
In:

The Magdeburg clinical studies' network for pediatric diseases.
In:

Nebenniere.
In:

Wachstum und Entwicklungsstörungen.
In:

Expression of components of the IGF signalling system in childhood acute lymphoblastic leukaemia.
In:

Glucagon therapy as a possible cause of erythema necrolyticum migrans in two neonates with persistent hyperinsulinaemic hypoglycaemia.
In:

Manifestation eines Cushing-Syndroms und osteoporotischer Frakturen in der Schwangerschaft einer Patientin mit Carney-Komplex.
In: