Ingeborg Krägeloh Mann


Ontology type: schema:Person     


Person Info

NAME

Ingeborg

SURNAME

Krägeloh Mann

Publications in SciGraph latest 50 shown

  • 2019 Nervensystem in PÄDIATRIE
  • 2018-11 De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-01 Bestmögliche kinderärztliche Versorgung der Bevölkerung in MONATSSCHRIFT KINDERHEILKUNDE
  • 2016-12 Brain morphometry in Pontocerebellar Hypoplasia type 2 in ORPHANET JOURNAL OF RARE DISEASES
  • 2015 Zerebralparesen in PÄDIATRIE
  • 2014-12 Natural course of pontocerebellar hypoplasia type 2A in ORPHANET JOURNAL OF RARE DISEASES
  • 2014-12 Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort in ORPHANET JOURNAL OF RARE DISEASES
  • 2014-12 Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts in ORPHANET JOURNAL OF RARE DISEASES
  • 2014 Zerebralparesen in PÄDIATRIE
  • 2013-03 Juvenile metachromatic leukodystrophy 10 years post transplant compared with a non-transplanted cohort in BONE MARROW TRANSPLANTATION
  • 2013-02 Schwere einer Epilepsie in ZEITSCHRIFT FÜR EPILEPTOLOGIE
  • 2013 Nervensystem in PÄDIATRIE
  • 2011-10 Metachromatic leukodystrophy: natural course of cerebral MRI changes in relation to clinical course in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2011-08 Therapie des Status epilepticus in MONATSSCHRIFT KINDERHEILKUNDE
  • 2010-09 Trends in prevalence of cerebral palsy in children born with a birthweight of 2,500 g or over in Europe from 1980 to 1998 in EUROPEAN JOURNAL OF EPIDEMIOLOGY
  • 2009-08 Grafikgestützter Konsensus für die Behandlung von Bewegungsstörungen bei Kindern mit bilateralen spastischen Zerebralparesen (BS-CP) in MONATSSCHRIFT KINDERHEILKUNDE
  • 2009 Nervensystem in PÄDIATRIE
  • 2008-09 tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia in NATURE GENETICS
  • 2007-08 Management des refraktären Status epilepticus in DER NERVENARZT
  • 2007-04 Global and local development of gray and white matter volume in normal children and adolescents in EXPERIMENTAL BRAIN RESEARCH
  • 2007-04 Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation in NATURE GENETICS
  • 2007-04 Brain Representation of Active and Passive Hand Movements in Children in PEDIATRIC RESEARCH
  • 2007 Perinatale Schädigungen des Nervensystems und so genannte Zerebralparesen in THERAPIE DER KRANKHEITEN IM KINDES- UND JUGENDALTER
  • 2006-07 Schütteltrauma in MONATSSCHRIFT KINDERHEILKUNDE
  • 2005 Nervensystem in PÄDIATRIE
  • 2004 Perinatale Schädigungen des Nervensystems und so genannte Zerebralparesen in THERAPIE DER KRANKHEITEN IM KINDES- UND JUGENDALTER
  • 2004-01 Benigne Partialepilepsie des Kleinkindesalters (Watanabe) in MONATSSCHRIFT KINDERHEILKUNDE
  • 2003-03 Malformations of the midline commissures: MRI findings in different forms of callosal dysgenesis in EUROPEAN RADIOLOGY
  • 2002-11 Zur Diskussion um die so genannten Zerebralparesen in MONATSSCHRIFT KINDERHEILKUNDE
  • 2002-10 Die neurologische und kognitive Entwicklung zu klein geborener Kinder in MONATSSCHRIFT KINDERHEILKUNDE
  • 2002-02 Congenital disorder of glycosylation type Ia: benign clinical course in a new genetic variant in CHILD'S NERVOUS SYSTEM
  • 2001 Nervensystem in PÄDIATRIE
  • 2001 Krankheiten des Nervensystems in PÄDIATRIE
  • 1999-04 Carbohydrate-deficient glycoprotein syndrome type 2 in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1994-09 Brain magnetic resonance imaging in children with optimally controlled hyperphenylalaninaemia in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1992-10 Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromes in EUROPEAN JOURNAL OF PEDIATRICS
  • 1992 Lissenzephalie-Komplex: MRI-Merkmale, Klinik, Anfallsspektrum, EEG und Entwicklung in AKTUELLE NEUROPÄDIATRIE 1991
  • 1992 Erste Ergebnisse einer epidemiologischen Untersuchung zur Nosologie der spastischen Tetraparesen in AKTUELLE NEUROPÄDIATRIE 1991
  • 1992 Transitorische neurologische Syndrome im ersten Lebensjahr in AKTUELLE NEUROPÄDIATRIE 1991
  • 1992 Spastische Tetraparese — Ätiologiediskussion anhand von kernspintomographischen Befunden in AKTUELLE NEUROPÄDIATRIE 1991
  • 1991 Volumenselektive Protonen-Spektroskopie des Gehirns bei Kindern mit neurodegenerativen Erkrankungen in AKTUELLE NEUROPÄDIATRIE 1990
  • 1991 Die Bedeutung der Kernspintomographie (MRT) bei der Diagnose des Morbus Pelizaeus-Merzbacher (MPM) in AKTUELLE NEUROPÄDIATRIE 1990
  • 1990 Tremor als Leitsymptom im Rahmen progredienter Enzephalopathie-Syndrome — Kasuistik und Differentialdiagnose in AKTUELLE NEUROPÄDIATRIE 1989
  • 1990 Defekt des Komplexes I der Atmungskette — Therapie und Verlauf in AKTUELLE NEUROPÄDIATRIE 1989
  • 1989 Beurteilung der motorischen Entwicklung im frühen Kindesalter in NORMALE UND GESTÖRTE ENTWICKLUNG
  • 1989 Das Rett-Syndrom: Klinische und kernspintomographische Befunde in AKTUELLE NEUROPÄDIATRIE 1988
  • 1989 Ataxia teleangiectatica (Louis-Bar) — Möglichkeiten früher Diagnostik in AKTUELLE NEUROPÄDIATRIE 1988
  • 1989 Theorie und Praxis krankengymnastischer Methoden auf neurophysiologischer Grundlage in NORMALE UND GESTÖRTE ENTWICKLUNG
  • 1989 Fehldiagnose „hypotone Zerebralparese“ bei der kongenitalen Form der myotonen Dystrophie in AKTUELLE NEUROPÄDIATRIE 1988
  • 1989 Drei Fälle von Hypomelanosis Ito mit Verlaufskontrolle in AKTUELLE NEUROPÄDIATRIE 1988
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