I. Krägeloh-Mann

发表

Recognition of Point-Light Biological Motion Displays by Young Children

N. Birbaumer, M. Pavlova, A. Sokolov, 2001, Perception.

Trends in prevalence of cerebral palsy in children born with a birthweight of 2,500 g or over in Europe from 1980 to 1998

I. Krägeloh-Mann, E. Sellier, G. Surman, 2010, European Journal of Epidemiology.

Brain Representation of Active and Passive Hand Movements in Children

M. Erb, G. Cioni, M. Wilke, 2007, Pediatric Research.

Introduction: Thyroid Function and Thyroid Therapy in the Premature Infant

C. Poets, I. Krägeloh-Mann, M. Ranke, 2007 .

Early left periventricular brain lesions induce right hemispheric organization of speech

M Erb, W Grodd, D Wildgruber, 2001, Neurology.

Increases in language lateralization in normal children as observed using magnetoencephalography

W. Lutzenberger, M. Wilke, I. Krägeloh-Mann, 2008, Brain and Language.

Brain lesions in preterms: origin, consequences and compensation

O. Pryds, I. Krägeloh-Mann, P. Toft, 1999, Acta paediatrica.

Imaging of early brain injury and cortical plasticity

Ingeborg Krägeloh-Mann, I. Krägeloh-Mann, 2004, Experimental Neurology.

Biological motion processing in adolescents with early periventricular brain damage

Marina Pavlova, Ingeborg Krägeloh-Mann, Niels Birbaumer, 2006, Neuropsychologia.

Language comprehension vs. language production: Age effects on fMRI activation

W. Grodd, M. Wilke, I. Krägeloh-Mann, 2011, Brain and Language.

Gender Affects Body Language Reading

M. Pavlova, P. Enck, I. Krägeloh-Mann, 2011, Front. Psychol..

Bilateral lesions of thalamus and basal ganglia: origin and outcome

I. Mader, F. Groenendaal, I. Krägeloh-Mann, 2002 .

Bilateral lesions of thalamus and basal ganglia: origin and outcome.

I. Mader, F. Groenendaal, I. Krägeloh-Mann, 2002, Developmental medicine and child neurology.

The role of magnetic resonance imaging in elucidating the pathogenesis of cerebral palsy: a systematic review

I. Krägeloh-Mann, V. Horber, 2007, Developmental medicine and child neurology.

Cerebral palsy update

Ingeborg Krägeloh-Mann, Christine Cans, I. Krägeloh-Mann, 2009, Brain and Development.

Assessing White Matter Microstructure in Brain Regions with Different Myelin Architecture Using MRI

Oliver Bieri, Klaus Scheffler, Ingeborg Krägeloh-Mann, 2016, PloS one.

Limitations on the developing preterm brain: impact of periventricular white matter lesions on brain connectivity and cognition.

Ingeborg Krägeloh-Mann, Marina A Pavlova, M. Pavlova, 2013, Brain : a journal of neurology.

Emotion through Locomotion: Gender Impact

Alexander N. Sokolov, Ingeborg Krägeloh-Mann, Marina A. Pavlova, 2013, PloS one.

Perception and production of biological movement in patients with early periventricular brain lesions.

Marina Pavlova, Ingeborg Krägeloh-Mann, Niels Birbaumer, 2003, Brain : a journal of neurology.

Recruitment of periventricular parietal regions in processing cluttered point-light biological motion.

Marina Pavlova, Ingeborg Krägeloh-Mann, Niels Birbaumer, 2005, Cerebral cortex.

Social interaction revealed by motion: dynamics of neuromagnetic gamma activity.

Werner Lutzenberger, Marina Pavlova, Michele Guerreschi, 2010, Cerebral cortex.

Combined functional and causal connectivity analyses of language networks in children: A feasibility study

Ingeborg Krägeloh-Mann, Marko Wilke, Karen Lidzba, 2009, Brain and Language.

Relationship between functional connectivity and sensory impairment: Red flag or red herring?

M. Wilke, S. Groeschel, I. Krägeloh-Mann, 2012, Human brain mapping.

Comprehensive language mapping in children, using functional magnetic resonance imaging: what's missing counts

Wolfgang Grodd, Ingeborg Krägeloh-Mann, Marko Wilke, 2005, Neuroreport.

Coherent corticomuscular oscillations originate from primary motor cortex: Evidence from patients with early brain lesions

Ingeborg Krägeloh-Mann, Christoph Braun, Johannes Dichgans, 2006, Human brain mapping.

Searching for motor functions in dysgenic cortex: a clinical transcranial magnetic stimulation and functional magnetic resonance imaging study.

C. Gerloff, W. Grodd, I. Krägeloh-Mann, 2004, Journal of neurosurgery.

Processing of non-canonical word-order: A case-series on lesion-induced reorganized language and age-effects in typical development

I. Krägeloh-Mann, S. Winkler, K. Lidzba, 2013, Brain and Language.

Decreasing prevalence in cerebral palsy: a multi‐site European population‐based study, 1980 to 2003

Ingeborg Krägeloh-Mann, Mary Jane Platt, Christine Cans, 2016, Developmental medicine and child neurology.

Growth in very preterm children: Head growth after discharge is the best independent predictor for cognitive outcome.

I. Krägeloh-Mann, K. Lidzba, A. Bevot, 2016, Early Human Development.

Clinical application of advanced MR methods in children: points to consider

M. Wilke, S. Groeschel, I. Krägeloh-Mann, 2018, Annals of clinical and translational neurology.

Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts

S. Züchner, P. Bauer, R. Schüle, 2014, Orphanet Journal of Rare Diseases.

Late onset Krabbe disease due to the new GALC p.Ala543Pro mutation, with intriguingly high residual GALC activity in vitro.

I. Krägeloh-Mann, K. Rostásy, A. Bornemann, 2017, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Review article Cerebral palsy update

I. Krägeloh-Mann, C. Cans, 2009 .

In vivo assessment of N-acetylaspartate in brain in spongy degeneration (Canavan's disease) by proton spectroscopy

W. Grodd, I. Krägeloh-Mann, D. Petersen, 1990, The Lancet.

Functional MRI in a 6-year-old boy with unilateral cortical malformation: concordant representation of both hands in the unaffected hemisphere.

W. Grodd, P. Winkler, I. Krägeloh-Mann, 2001, Neuropediatrics.

Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.

F. Baas, D. Ferriero, J. Graham, 2011, Brain : a journal of neurology.

Cerebrospinal fluid pterins and folates in Aicardi-Goutières syndrome

I. Krägeloh-Mann, N. Blau, V. Ramaekers, 2003, Neurology.

Measurement of volume of cerebral blood flow in healthy preterm and term neonates with ultrasound

I. Krägeloh-Mann, M. Schöning, R. Goelz, 2002, The Lancet.

Plasticity during Early Brain Development Is Determined by Ontogenetic Potential

M. Wilke, M. Pavlova, I. Krägeloh-Mann, 2017, Neuropediatrics.

Lesion characteristics driving right-hemispheric language reorganization in congenital left-hemispheric brain damage

M. Wilke, I. Krägeloh-Mann, M. Staudt, 2017, Brain and Language.

Trends in cerebral palsy among infants of very low birthweight:a database study

I. Krägeloh-Mann, G. Surman, C. Cans, 2007 .

The Mutation Matters: CSF Profiles of GCase, Sphingolipids, α‐Synuclein in PDGBA

D. Galasko, D. Berg, B. Mollenhauer, 2021, Movement disorders : official journal of the Movement Disorder Society.

Schoolchildren born VLBW or VLGA show height-related changes in body composition and muscle function but no evidence of metabolic syndrome risk factors. Results from the NEOLONG study

I. Krägeloh-Mann, H. Wollmann, G. Binder, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Arithmetic and brain connectivity: Mental calculation in adolescents with periventricular lesions

M. Pavlova, A. Sokolov, I. Krägeloh-Mann, 2009, Neuropsychologia.

The role of magnetic resonance imaging in furthering understanding of the pathogenesis of cerebral palsy.

I. Krägeloh-Mann, V. Horber, 2007, Developmental medicine and child neurology.

(Re-)organization of basal ganglia in congenital hemiparesis with ipsilateral cortico-spinal projections.

W. Grodd, I. Krägeloh-Mann, M. Staudt, 2008, Neuropediatrics.

Impact of Hippotherapy on Gross Motor Function and Quality of Life in Children with Bilateral Cerebral Palsy: A Randomized Open-Label Crossover Study

I. Krägeloh-Mann, N. Heussen, T. Polster, 2018, Neuropediatrics.

MRI classification system (MRICS) for children with cerebral palsy: development, reliability, and recommendations

I. Krägeloh-Mann, K. Himmelmann, V. Horber, 2017, Developmental medicine and child neurology.

Early determination of somatosensory cortex in the human brain.

B. de Haan, H. Karnath, I. Krägeloh-Mann, 2011, Cerebral cortex.

Metachromatic leukodystrophy: natural course of cerebral MRI changes in relation to clinical course

W. Grodd, S. Groeschel, I. Krägeloh-Mann, 2011, Journal of Inherited Metabolic Disease.

Microstructure of transcallosal motor fibers reflects type of cortical (re-)organization in congenital hemiparesis.

M. Shenton, F. Heinen, I. Krägeloh-Mann, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Niemann-Pick type C is frequent in adult ataxia with cognitive decline and vertical gaze palsy

P. Bauer, L. Schöls, I. Krägeloh-Mann, 2013, Neurology.

Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C

A. Vanderver, R. Schiffmann, D. Timmann, 2020, The Journal of clinical endocrinology and metabolism.

Growth and Development are Similar in VLBW Children Born Appropriate and Small for Gestational Age: An Interim Report on 97 Preschool Children

I. Krägeloh-Mann, H. Wollmann, M. Ranke, 2007, Journal of pediatric endocrinology & metabolism : JPEM.

Author Response: Association of Age at Onset and First Symptoms With Disease Progression in Patients With Metachromatic Leukodystrophy

S. Groeschel, I. Krägeloh-Mann, 2021, Neurology.

Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults

L. Schöls, I. Krägeloh-Mann, A. Rolfs, 2010, Brain and Development.

Identification of neurodegeneration indicators and disease progression in metachromatic leukodystrophy using quantitative NMR‐based urinary metabolomics

S. Groeschel, I. Krägeloh-Mann, M. Spraul, 2022, JIMD reports.

Early clinical course after hematopoietic stem cell transplantation in children with juvenile metachromatic leukodystrophy

S. Groeschel, I. Krägeloh-Mann, A. Grimm, 2020, Molecular and Cellular Pediatrics.

Prospective cohort study of mortality in very low birthweight infants in a single centre in the Eastern Cape province, South Africa

I. Krägeloh-Mann, E. Jordaan, M. Mazinu, 2021, BMJ Paediatrics Open.

Cerebral manifestation of Wilson's disease successfully treated with liver transplantation

H. Hefter, I. Krägeloh-Mann, P. Neuhaus, 1998, Neurology.

Antiphospholipid Antibodies in Cerebrovascular Ischemia and Stroke in Childhood

I. Krägeloh-Mann, M. Schöning, R. Michaelis, 1994, Neuropediatrics.

Postnatal human cytomegalovirus infection in preterm infants has long-term neuropsychological sequelae.

Katharina F. Brecht, M. Wilke, I. Krägeloh-Mann, 2015, Jornal de Pediatria.

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia.

S. Mane, T. Nägele, T. Meitinger, 2020, American journal of human genetics.

SERAC1 deficiency causes complicated HSP: evidence from a novel splice mutation in a large family

T. Meitinger, B. Bender, R. Schüle, 2017, Journal of Medical Genetics.

Pontocerebellar hypoplasia type 2: variability in clinical and imaging findings.

D. Zafeiriou, I. Krägeloh-Mann, E. Boltshauser, 2007, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromes

F. Hanefeld, I. Krägeloh-Mann, J. Fryns, 1992, European Journal of Pediatrics.

Human organoid model of PCH2a recapitulates brain region-specific pathology

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2022, bioRxiv.

Alexander disease--classification revisited and isolation of a neonatal form.

W. Grodd, D. Auer, I. Krägeloh-Mann, 2000, Neuropediatrics.

The cognitive outcome of very preterm children: how to interpret results

I. Krägeloh-Mann, AF Williams, 2002, Acta paediatrica.

Metachromatic Leukodystrophy – An Update

I. Krägeloh-Mann, V. Gieselmann, 2010, Neuropediatrics.

PROTON SPECTROSCOPY IN FIVE PATIENTS WITH LEIGH'S DISEASE AND MITOCHONDRIAL ENZYME DEFICIENCY

W. Grodd, T. Nägele, I. Krägeloh-Mann, 1993, Developmental medicine and child neurology.

Assessment and therapy monitoring of Leigh disease by MRI and proton spectroscopy.

W. Grodd, I. Krägeloh-Mann, G. Niemann, 1992, Pediatric neurology.

Preserved crossed corticospinal tract and hand function despite extensive brain maldevelopment.

W. Grodd, I. Krägeloh-Mann, M. Staudt, 2009, Pediatric neurology.

Pyramidal tract damage correlates with motor dysfunction in bilateral periventricular leukomalacia (PVL).

W. Grodd, M. Pavlova, I. Krägeloh-Mann, 2003, Neuropediatrics.

Acute-onset paralytic strabismus in toddlers is important to consider as a potential early sign of late-infantile Metachromatic Leukodystrophy.

S. Groeschel, I. Krägeloh-Mann, M. S. van der Knaap, 2022, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Safety of intrathecal delivery of recombinant human arylsulfatase A in children with metachromatic leukodystrophy: Results from a phase 1/2 clinical trial.

I. Krägeloh-Mann, R. Giugliani, N. Sakai, 2020, Molecular genetics and metabolism.

Phenotypic variation between siblings with Metachromatic Leukodystrophy

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2019, Orphanet Journal of Rare Diseases.

Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Juvenile Metachromatic Leukodystrophy Compared With Nontransplanted Control Patients.

B. Weschke, S. Groeschel, I. Krägeloh-Mann, 2016, JAMA neurology.

Juvenile metachromatic leukodystrophy 10 years post transplant compared with a non-transplanted cohort

T. Nägele, S. Groeschel, I. Krägeloh-Mann, 2013, Bone Marrow Transplantation.

Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? - Chances and challenges.

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2022, Molecular genetics and metabolism.

Motor dysfunction in NF1: Mediated by attention deficit or inherent to the disorder?

I. Krägeloh-Mann, V. Mautner, K. Lidzba, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Hereditary diffuse leukoencephalopathy with spheroids (HDLS) with a novel CSF1R mutation and spinal cord involvement

H. Heinze, P. Nestor, I. Krägeloh-Mann, 2015, Journal of the Neurological Sciences.

Grey matter injury in cerebral palsy – pallidum for the role of the predicting severity

I. Krägeloh-Mann, 2015, Developmental medicine and child neurology.

Reply: Periventricular leukomalacia disrupts brain connectivity

C. Braun, M. Pavlova, A. Sokolov, 2006 .

The Rett syndrome: Magnetic resonance imaging and clinical findings in four girls

G. Schroth, I. Krägeloh-Mann, G. Niemann, 1989, Brain and Development.

PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution

J. Shendure, Martin Kircher, K. Devriendt, 2016, JCI insight.

Misleading functional magnetic resonance imaging mapping of the cortical hand representation in a 4-year-old boy with an arteriovenous malformation of the central region.

C. Braun, I. Krägeloh-Mann, M. Staudt, 2009, Journal of neurosurgery. Pediatrics.

Two types of ipsilateral reorganization in congenital hemiparesis: a TMS and fMRI study.

Michael Erb, Wolfgang Grodd, Ingeborg Krägeloh-Mann, 2002, Brain : a journal of neurology.

Specific impairment of functional connectivity between language regions in former early preterms

Ingeborg Krägeloh-Mann, Marko Wilke, Till-Karsten Hauser, 2014, Human brain mapping.

Cerebral gray and white matter changes and clinical course in metachromatic leukodystrophy

C. Krarup, M. Wilke, S. Groeschel, 2012, Neurology.

Clinical functional MRI of the language domain in children with epilepsy

Wolfgang Grodd, Marko Wilke, Martin Staudt, 2011, Human brain mapping.

Somatosensory system in two types of motor reorganization in congenital hemiparesis: Topography and function

Wolfgang Grodd, Ingeborg Krägeloh-Mann, Christoph Braun, 2009, Human brain mapping.

[Biotinidase deficiency: a congenital metabolic disease which can be successfully treatment with vitamin H].

T. Suormala, E. R. Baumgartner, I. Krägeloh-Mann, 1989, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde.

A Mutation-Agnostic Hematopoietic Stem Cell Gene Therapy for Metachromatic Leukodystrophy.

I. Krägeloh-Mann, R. Handgretinger, Jennifer Rottenberger, 2021, The CRISPR journal.

Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation: clinical and genetic characterization and target for therapy

I. Krägeloh-Mann, G. Scheper, M. Knaap, 2014 .

Interrater reliability study of cerebral palsy diagnosis, neurological subtype, and gross motor function

I. Krägeloh-Mann, E. Sellier, C. Cans, 2012, Developmental medicine and child neurology.

Development and reliability of a classification system for gross motor function in children with metachromatic leucodystrophy

I. Krägeloh-Mann, G. Blumenstock, C. Kehrer, 2011, Developmental medicine and child neurology.

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

L. Lagae, P. Striano, T. Loddenkemper, 2017, Brain : a journal of neurology.

Brain magnetic resonance imaging in children with optimally controlled hyperphenylalaninaemia

I. Krägeloh-Mann, P. Guldberg, O. Henriksen, 1994, Journal of Inherited Metabolic Disease.

Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome.

A. Schulz, S. Ehl, H. Hennies, 2016, Blood.

Defining the phenotypical spectrum associated with variants in TUBB2A

D. Wieczorek, I. Krägeloh-Mann, G. Mancini, 2020, Journal of Medical Genetics.

Prosaposin Deficiency and Saposin B Deficiency (Activator-Deficient Metachromatic Leukodystrophy): Report on Two Patients Detected by Analysis of Urinary Sphingolipids and Carrying Novel PSAP Gene Mutations

I. Krägeloh-Mann, M. Staudt, M. Elleder, 2009, American journal of medical genetics. Part A.

The European Reference Network for Rare Neurological Diseases

E. Bertini, R. Vandenberghe, L. Schöls, 2021, Frontiers in Neurology.

Measurement of recombinant human arylsulfatase A and leukocyte sulfatase activities by analytical isotachophoresis.

I. Krägeloh-Mann, G. Bruchelt, J. Böhringer, 2019, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Long‐term outcome in preterm children with human cytomegalovirus infection transmitted via breast milk

Ingeborg Krägeloh-Mann, Brigitte Vollmer, I. Krägeloh-Mann, 2012, Acta paediatrica.

Pontocerebellar hypoplasia type 11: Does the genetic defect determine timing of cerebellar pathology?

S. Groeschel, I. Krägeloh-Mann, M. Sturm, 2020, European journal of medical genetics.

Medical, Psychological and Intellectual Development of 5-Year-Old Children Born after Intracytoplasmic Sperm Injection

I. Krägeloh-Mann, U. Mau-Holzmann, K. Lidzba, 2011, Neuropediatrics.

Increased frequency of severe major anomalies in children conceived by intracytoplasmic sperm injection

I. Krägeloh-Mann, U. Mau-Holzmann, P. Licht, 2007, Developmental medicine and child neurology.

Transitory neurological findings in a population of at risk infants.

I. Krägeloh-Mann, R. Michaelis, G. Haas, 1993, Early human development.

In vitro analysis of multipotent mesenchymal stromal cells as potential cellular therapeutics in neurometabolic diseases in pediatric patients.

I. Krägeloh-Mann, R. Handgretinger, G. Bruchelt, 2006, Experimental hematology.

Growth, head growth, and neurocognitive outcome in children born very preterm: methodological aspects and selected results

I. Krägeloh-Mann, M. Ranke, B. Vollmer, 2015, Developmental medicine and child neurology.

Effects of Liberal vs Restrictive Transfusion Thresholds on Survival and Neurocognitive Outcomes in Extremely Low-Birth-Weight Infants: The ETTNO Randomized Clinical Trial.

C. Poets, R. Rossi, I. Krägeloh-Mann, 2020, JAMA.

What constitutes cerebral palsy in the twenty‐first century?

I. Krägeloh-Mann, K. Himmelmann, C. Cans, 2014, Developmental medicine and child neurology.

De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function

S. Züchner, P. Bauer, R. Schüle, 2018, European Journal of Human Genetics.

Cerebral palsy and congenital malformations.

Ester Garne, Christine Cans, E. Garne, 2008, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Natural history of Krabbe disease – a nationwide study in Germany using clinical and MRI data

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2020, Orphanet Journal of Rare Diseases.

De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophy.

T. Meitinger, I. Krägeloh-Mann, R. Płoski, 2020, Brain : a journal of neurology.

Microcephaly with simplified gyral pattern

Ingeborg Krägeloh-Mann, Marko Wilke, M. Wilke, 2010, Neurology.

tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia

Ingeborg Krägeloh-Mann, Francesco Muntoni, Peter Nürnberg, 2008, Nature Genetics.

Spasmodic Abdominal Pain and Other Gastrointestinal Symptoms in Pontocerebellar Hypoplasia Type 2

I. Krägeloh-Mann, H. Schaefer, T. Langer, 2021, Neuropediatrics.

Brain morphometry in Pontocerebellar Hypoplasia type 2

Ingeborg Krägeloh-Mann, Samuel Groeschel, Corinna Engel, 2014, Orphanet Journal of Rare Diseases.

Natural course of pontocerebellar hypoplasia type 2A

I. Krägeloh-Mann, P. Barth, M. Steinlin, 2014, Orphanet Journal of Rare Diseases.

CNS infections: progress in therapy, diagnosis, and prevention

I. Krägeloh-Mann, 2008 .

Preterm Cognitive outcome and socioeconomic status

I. Krägeloh-Mann, K. Lidzba, 2012, Acta paediatrica.

Understanding causation of cerebral palsy by using magnetic resonance imaging

I. Krägeloh-Mann, 2008 .

Paediatric neurology: traditional opinions revisited

I. Krägeloh-Mann, 2008, The Lancet Neurology.

Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation

R. Schiffmann, I. Krägeloh-Mann, C. Florentz, 2007, Nature Genetics.

A new leukoencephalopathy with brainstem and spinal cord involvement and high lactate

F. Barkhof, P. Pouwels, I. Krägeloh-Mann, 2003, Annals of neurology.

Enzymatic characterization of novel arylsulfatase A variants using human arylsulfatase A‐deficient immortalized mesenchymal stromal cells

L. Schöls, I. Krägeloh-Mann, R. Handgretinger, 2017, Human mutation.

Global and local development of gray and white matter volume in normal children and adolescents

Ingeborg Krägeloh-Mann, Marko Wilke, Scott K. Holland, 2007, Experimental Brain Research.

Demyelination load as predictor for disease progression in juvenile metachromatic leukodystrophy

M. Wilke, S. Groeschel, I. Krägeloh-Mann, 2017, Annals of clinical and translational neurology.

Acute Encephalopathy Associated with Vigabatrin in a Six‐Month‐Old Girl

I. Krägeloh-Mann, G. Niemann, M. Wolff, 2000, Epilepsia.

Brief Communication Acute Encephalopathy Associated with Vigabatrin in a Six-Month-Old Girl

I. Krägeloh-Mann, G. Niemann, M. Wolff, 2000 .

The Role of Neuroimaging and Genetic Analysis in the Diagnosis of Children With Cerebral Palsy

I. Krägeloh-Mann, E. Sellier, K. Himmelmann, 2021, Frontiers in Neurology.

Congenital disorder of glycosylation type Ia: benign clinical course in a new genetic variant

I. Mader, I. Krägeloh-Mann, W. Küker, 2002, Child's Nervous System.

Therapy Trial Design in Vanishing White Matter

Robert M. Rauner, A. Vanderver, R. Schiffmann, 2022, Neurology: Genetics.

POLR3A variants with striatal involvement and extrapyramidal movement disorder

I. Harting, P. Pouwels, I. Krägeloh-Mann, 2020, neurogenetics.

European consensus table 2006 on botulinum toxin for children with cerebral palsy.

K. Desloovere, G. Molenaers, F. Heinen, 2006, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

The updated European Consensus 2009 on the use of Botulinum toxin for children with cerebral palsy.

K. Desloovere, G. Molenaers, F. Heinen, 2010, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Biological Motion Shown Backwards: The Apparent-Facing Effect

Marina Pavlova, Ingeborg Krägeloh-Mann, Niels Birbaumer, 2002, Perception.

BILATERAL SPASTIC CEREBRAL PALSY‐MRI PATHOLOGY AND ORIGIN. ANALYSIS FROM A REPRESENTATIVE SERIES OF 56 CASES

I. Krägeloh-Mann, G. Hagberg, B. Vollmer, 1995, Developmental medicine and child neurology.

CONGENITAL HEMIPARESIS AND PERIVENTRICULAR LEUKOMALACIA PATHOGENETIC ASPECTS ON MAGNETIC RESONANCE IMAGING

W. Grodd, I. Krägeloh-Mann, G. Niemann, 1994, Developmental medicine and child neurology.

The impact of severe rare chronic neurological disease in childhood on the quality of life of families—a study on MLD and PCH2

S. Groeschel, I. Krägeloh-Mann, C. Kehrer, 2021, Orphanet Journal of Rare Diseases.

BILATERAL SPASTIC CEREBRAL PALSY‐A COLLABORATIVE STUDY BETWEEN SOUTHWEST GERMANY AND WESTERN SWEDEN. Ill: AETIOLOGY

C. Meisner, I. Krägeloh-Mann, G. Hagberg, 1995, Developmental medicine and child neurology.

Reorganization of the cerebro-cerebellar network of language production in patients with congenital left-hemispheric brain lesions

M. Wilke, W. Grodd, M. Wilke, 2008, Brain and Language.

Late Detection of Neuroblastoma in a Patient with Prolonged Cerebellar Ataxia without Opsoclonus

I. Krägeloh-Mann, G. Niemann, M. Schöning, 2001, Neuropediatrics.

Reorganization in congenital hemiparesis acquired at different gestational ages

Wolfgang Grodd, Martin Staudt, Christian Gerloff, 2004, Annals of neurology.

Growth of a cohort of very low birth weight and preterm infants born at a single tertiary health care center in South Africa

I. Krägeloh-Mann, E. Jordaan, M. Mazinu, 2023, Frontiers in Pediatrics.

A Mitochondrial Myopathy in an Infant with Lactic Acidosis

I. Krägeloh-Mann, W. Paulus, W. Ruitenbeek, 1990, Developmental medicine and child neurology.

Metabolic and destructive brain disorders in children: findings with localized proton MR spectroscopy.

U. Klose, W. Grodd, I. Krägeloh-Mann, 1991, Radiology.

Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypes

G. Vasco, S. Groeschel, A. Caglayan, 2021, Journal of Medical Genetics.

Dyskinetic cerebral palsy in Europe: trends in prevalence and severity

I. Krägeloh-Mann, K. Himmelmann, C. Cans, 2009, Archives of Disease in Childhood.

Visuospatial deficits in patients with early left-hemispheric lesions and functional reorganization of language: Consequence of lesion or reorganization?

Ingeborg Krägeloh-Mann, Marko Wilke, Martin Staudt, 2006, Neuropsychologia.

Developing somatosensory projections bypass periventricular brain lesions

M. Erb, C. Braun, C. Gerloff, 2006, Neurology.

Right-Hemispheric Organization of Language Following Early Left-Sided Brain Lesions: Functional MRI Topography

Wolfgang Grodd, Ingeborg Krägeloh-Mann, Michael Erb, 2002, NeuroImage.

Neuroimaging Patterns and Function in Cerebral Palsy—Application of an MRI Classification

I. Krägeloh-Mann, E. Sellier, K. Himmelmann, 2021, Frontiers in Neurology.

Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation

R. Schüle, I. Krägeloh-Mann, M. Lee-Kirsch, 2019, Neurology: Genetics.

BILATERAL SPASTIC CEREBRAL PALSY—A COMPARATIVE STUDY BETWEEN SOUTHWEST GERMANY AND WESTERN SWEDEN. I: CLINICAL PATTERNS AND DISABILITIES

C. Meisner, I. Krägeloh-Mann, G. Hagberg, 1993, Developmental medicine and child neurology.

CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis

S. Züchner, P. Bauer, R. Schüle, 2017, Neurology: Genetics.

Characterisation of Aicardi-Goutières syndrome

I. Krägeloh-Mann, 2013, The Lancet Neurology.

Neuromagnetic Response to Body Motion and Brain Connectivity

Marina Pavlova, Alexander N. Sokolov, Ingeborg Krägeloh-Mann, 2009, Journal of Cognitive Neuroscience.

Perception and Understanding of Others' Actions and Brain Connectivity

Marina Pavlova, Alexander N. Sokolov, Ingeborg Krägeloh-Mann, 2008, Journal of Cognitive Neuroscience.

Oscillatory MEG response to human locomotion is modulated by periventricular lesions

Werner Lutzenberger, Marina Pavlova, Ingeborg Krägeloh-Mann, 2007, NeuroImage.

Visual navigation in adolescents with early periventricular lesions: knowing where, but not getting there.

Marina Pavlova, Ingeborg Krägeloh-Mann, M. Pavlova, 2006, Cerebral cortex.

Periventricular leukomalacia specifically affects cortical MEG response to biological motion

Marina Pavlova, Ingeborg Krägeloh-Mann, Niels Birbaumer, 2006, Annals of neurology.

Functional topography of early periventricular brain lesions in relation to cytoarchitectonic probabilistic maps

Wolfgang Grodd, Ingeborg Krägeloh-Mann, Martin Staudt, 2008, Brain and Language.

Cerebral palsy: towards developmental neuroscience

I. Krägeloh-Mann, 2005 .

Cerebral palsy: towards developmental neuroscience.

I. Krägeloh-Mann, 2005, Developmental medicine and child neurology.

The pyramidal tract in congenital hemiparesis: relationship between morphology and function in periventricular lesions.

W Grodd, W. Grodd, I. Krägeloh-Mann, 2000, Neuropediatrics.

An fMRI task battery for assessing hemispheric language dominance in children

Wolfgang Grodd, Ingeborg Krägeloh-Mann, Karen Lidzba, 2006, NeuroImage.

Testing the language of German cerebral palsy patients with right hemispheric language organization after early left hemispheric damage

I. Krägeloh-Mann, S. Winkler, K. Lidzba, 2012, Clinical linguistics & phonetics.

Why one task is not enough: functional MRI for atypical language organization in two children.

Ingeborg Krägeloh-Mann, Marko Wilke, M. Wilke, 2010, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Language lateralization in magnetoencephalography: two tasks to investigate hemispheric dominance

Werner Lutzenberger, Hubert Preissl, Ingeborg Krägeloh-Mann, 2006, Neuroreport.

Development and lateralization of language in the presence of early brain lesions.

I. Krägeloh-Mann, K. Lidzba, 2005, Developmental medicine and child neurology.

Paradigms provoking right lateralized activation in fMRI

M. Erb, W. Grodd, M. Wilke, 2004 .

Letter to the Editor

I. Krägeloh-Mann, V. Horber, 2007 .

Cortical response to social interaction is affected by gender

Werner Lutzenberger, Marina Pavlova, Michele Guerreschi, 2010, NeuroImage.

Trends in Prevalence and Severity of Pre/Perinatal Cerebral Palsy Among Children Born Preterm From 2004 to 2010: A SCPE Collaboration Study

E. Ortibus, I. Krägeloh-Mann, E. Sellier, 2021, Frontiers in Neurology.

L-2 hydroxyglutaric aciduria as a rare cause of leukencephalopathy in adults

L. Schöls, I. Krägeloh-Mann, M. Schlamann, 2013, Clinical Neurology and Neurosurgery.

The second report of a new hypomyelinating disease due to a defect in the VPS11 gene discloses a massive lysosomal involvement

I. Krägeloh-Mann, S. Biskup, A. Bornemann, 2016, Journal of Inherited Metabolic Disease.

Magnetic Resonance Imaging Of The Brain Of Children With Multiple Sclerosis

G. Schroth, I. Krägeloh-Mann, G. Haas, 1987, Developmental medicine and child neurology.

Niemann-Pick disease type A and B are clinically but also enzymatically heterogeneous: pitfall in the laboratory diagnosis of sphingomyelinase deficiency associated with the mutation Q292 K.

P. Bauer, I. Krägeloh-Mann, A. Rolfs, 2003, Neuropediatrics.

Plasma Exchange Is Effective in a 13-Year-Old Girl with Steroid-Resistant Bilateral Optic Neuritis

I. Krägeloh-Mann, A. Melms, M. Wolff, 2013, Neuropediatrics.

Malformations of the midline commissures: MRI findings in different forms of callosal dysgenesis

T. Nägele, I. Mader, I. Krägeloh-Mann, 2003, European Radiology.

Proton MR spectroscopy reveals lactate in infantile neuroaxonal dystrophy (INAD).

W. Grodd, T. Nägele, I. Mader, 2001, Neuropediatrics.

Leukodystrophies underlying cryptic spastic paraparesis: frequency and phenotype in 76 patients

R. Schüle, L. Schöls, I. Krägeloh-Mann, 2014, European journal of neurology.

Leukodystrophies in idiopathic adult‐onset ataxia: Frequency and phenotype in 105 patients

L. Schöls, I. Krägeloh-Mann, M. Synofzik, 2013, Movement disorders : official journal of the Movement Disorder Society.

Lesion-induced right-hemispheric language and organization of nonverbal functions

Wolfgang Grodd, Marko Wilke, Martin Staudt, 2006, Neuroreport.

Generation of two iPSC lines derived from two unrelated patients with Gaucher disease.

R. Schüle, I. Krägeloh-Mann, J. Böhringer, 2019, Stem Cell Research.

T2-Pseudonormalization and Microstructural Characterization in Advanced Stages of Late-infantile Metachromatic Leukodystrophy

U. Klose, T. Nägele, K. Scheffler, 2020, Clinical Neuroradiology.

Optimization of Enzyme Essays to Enhance Reliability of Activity Measurements in Leukocyte Lysates for the Diagnosis of Metachromatic Leukodystrophy and Gangliosidoses

S. Groeschel, I. Krägeloh-Mann, Sebastian G Strobel, 2020, Cells.

Maternal perinatal depressive symptoms trajectories and impact on toddler behavior - the importance of symptom duration and maternal bonding.

I. Krägeloh-Mann, E. Fransson, A. Skalkidou, 2020, Journal of affective disorders.

Association of Age at Onset and First Symptoms With Disease Progression in Patients With Metachromatic Leukodystrophy

L. Schöls, S. Groeschel, I. Krägeloh-Mann, 2020, Neurology.

Metachromatic Leukodystrophy and Globoid Cell Leukodystrophy

I. Krägeloh-Mann, V. Gieselmann, D. Wenger, 2012 .

MR-spectroscopy in metachromatic leukodystrophy: A model free approach and clinical correlation

U. Klose, S. Groeschel, I. Krägeloh-Mann, 2022, NeuroImage: Clinical.

Intravenous arylsulfatase A in metachromatic leukodystrophy: a phase 1/2 study

C. Krarup, S. Groeschel, I. Krägeloh-Mann, 2020, Annals of clinical and translational neurology.

Therapies of lysosomal storage disorders targeting the brain

S. Groeschel, I. Krägeloh-Mann, 2016, The Lancet.

Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort

S. Groeschel, I. Krägeloh-Mann, V. Gieselmann, 2014, Orphanet Journal of Rare Diseases.

The natural course of gross motor deterioration in metachromatic leukodystrophy

I. Krägeloh-Mann, V. Gieselmann, G. Blumenstock, 2011, Developmental medicine and child neurology.

Recognizing early MRI signs (or their absence) is crucial in diagnosing metachromatic leukodystrophy

S. Groeschel, I. Krägeloh-Mann, M. S. van der Knaap, 2022, Annals of clinical and translational neurology.

Enlargement of peripheral nerves in Krabbe disease: The diagnostic value of nerve ultrasound

T. Nägele, S. Groeschel, I. Krägeloh-Mann, 2020, Muscle & nerve.

Severity of Cerebral Palsy—The Impact of Associated Impairments

I. Krägeloh-Mann, E. Sellier, C. Arnaud, 2020, Neuropediatrics.

The Origin of the Cerebral Palsies: Contribution of Population-Based Neuroimaging Data

E. Ortibus, I. Krägeloh-Mann, E. Sellier, 2020, Neuropediatrics.

The reference and training manual of the SCPE (surceillance of cerebral palsy in europe)

I. Krägeloh-Mann, P. Weber, U. Petruch, 2004 .

Case gender and severity in cerebral palsy varies with intrauterine growth

I. Krägeloh-Mann, C. Cans, P. Uvebrant, 2005, Archives of Disease in Childhood.

Decreasing cerebral palsy prevalence in multiple births in the modern era: a population cohort study of European data

I. Krägeloh-Mann, E. Sellier, J. Rankin, 2020, Archives of Disease in Childhood.

Long‐term disease course of two patients with multiple sulfatase deficiency differs from metachromatic leukodystrophy in a broad cohort

S. Groeschel, I. Krägeloh-Mann, T. Haack, 2020, JIMD reports.

Rare Variant of GM2 Gangliosidosis through Activator-Protein Deficiency

I. Krägeloh-Mann, R. Trollmann, J. Böhringer, 2017, Neuropediatrics.

De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function

S. Züchner, P. Bauer, R. Schüle, 2018, European Journal of Human Genetics.

Congenital bilateral perisylvian syndrome (CBPS): do concomitant esophageal malformations indicate a poor prognosis?

I. Krägeloh-Mann, J. Riethmüller, W. Küker, 2000, Neuropediatrics.

PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution

Martin, J. Shendure, Martin Kircher, 2016, JCI insight.

The development of cerebral perfusion in healthy preterm and term neonates.

I. Krägeloh-Mann, M. Schöning, R. Goelz, 2003, Neuropediatrics.

Bilateral spastic cerebral palsy--pathogenetic aspects from MRI.

I. Krägeloh-Mann, B. Hagberg, R. Michaelis, 1992, Neuropediatrics.

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN 2 A-related disorders

L. Lagae, P. Striano, T. Loddenkemper, 2017 .

Core protocol development for phase 2/3 clinical trials in the leukodystrophy vanishing white matter: a consensus statement by the VWM consortium and patient advocates

Robert M. Rauner, A. Vanderver, A. Fatemi, 2023, BMC Neurology.

FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.

S. Züchner, P. Bauer, R. Schüle, 2019, Brain : a journal of neurology.

Hematopoietic stem cell transplantation with mesenchymal stromal cells in children with metachromatic leukodystrophy.

S. Groeschel, I. Krägeloh-Mann, R. Handgretinger, 2022, Stem cells and development.

What constitutes cerebral palsy in the twenty‐first century?

I. Krägeloh-Mann, K. Himmelmann, C. Cans, 2014, Developmental medicine and child neurology.

Motor dysfunction in NF1: Mediated by attention deficit or inherent to the disorder?

I. Krägeloh-Mann, V. Mautner, K. Lidzba, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Language comprehension vs. language production: Age effects on fMRI activation

W. Grodd, M. Wilke, I. Krägeloh-Mann, 2011, Brain and Language.

Somatosensory system in two types of motor reorganization in congenital hemiparesis: Topography and function

C. Braun, W. Grodd, M. Wilke, 2009, Human brain mapping.

Hypomelanosis of Ito - Report of Four Cases and Survey of the Literature

I. Krägeloh-Mann, R. Michaelis, Verena Griebel, 1989, Neuropediatrics.

Ipsilateral corticospinal pathways in congenital hemiparesis on routine magnetic resonance imaging.

W. Grodd, I. Krägeloh-Mann, M. Staudt, 2005, Pediatric neurology.

2-Jahres-Nachuntersuchung (Bayley) sehr kleiner Frühgeborener der Jahrgänge 2004–2007: Ergebnisse und Vollständigkeitsanalyse eines Perinatalzentrums

C. Poets, I. Krägeloh-Mann, M. Schöning, 2010, Klinische Padiatrie.

Hematopoietic Stem Cell Therapy In Eight Patients with Metachromatic Leukodystrophy – Relevance of Post-Transplant Medication.

I. Krägeloh-Mann, A. Erbacher, R. Handgretinger, 2010 .