Birgit Spors
Berlin, BE, Germany
Last Updated: 09/26/2026
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Found 27 publications
Greater maltreatment severity is associated with smaller brain volume with implication for intellectual ability in young children.
Journal: Neurobiology of stress
Published: June 05, 2023
Standard values for MRI brain biometry throughout the first year of life.
Journal: Pediatrics and neonatology
Published: November 22, 2020
Brain malformations and cognitive performance in spina bifida.
Journal: Developmental medicine and child neurology
Published: September 29, 2020
Age-specific occurrence of pathological fractures in patients with spina bifida.
Journal: European journal of pediatrics
Published: April 26, 2019
Primary oral manifestation of Langerhans cell histiocytosis refractory to conventional therapy but susceptible to BRAF-specific treatment: a case report and review of the literature.
Journal: Therapeutic advances in medical oncology
Published: March 30, 2019
Potential Risks to Stable Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation for Children With Cerebral X-linked Adrenoleukodystrophy.
Journal: JAMA network open
Published: January 16, 2019
A comparison study of anxiety in children undergoing brain MRI vs adults undergoing brain MRI vs children undergoing an electroencephalogram.
Journal: PloS one
Published: June 09, 2018
Lymphatic malformation with acquired Horner syndrome in an infant.
Journal: BMJ case reports
Published: October 26, 2017
Lymphatic malformation with acquired Horner syndrome in an infant.
Journal: Journal of neurointerventional surgery
Published: July 11, 2017
Erratum to: Risk of cancer incidence before the age of 15 years after exposure to ionising radiation from computed tomography: results from a German cohort study.
Journal: Radiation and environmental biophysics
Published: June 15, 2017
Acute isolated partial oculomotor nerve palsy due to Lyme neuroborreliosis in a 5 year old girl.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: September 10, 2015
An overlapping phenotype of Osteogenesis imperfecta and Ehlers-Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencing.
Journal: American journal of medical genetics. Part A
Published: April 27, 2015
Last Updated: 09/26/2026