Related Experiment Videos
Summary
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Imaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spaces.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society·2017
Sixteenth-century German woodcut of a male infant with possible disorganization.
Clinical genetics·2015
In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome.
Journal of medical genetics·2003
Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes.
Lancet (London, England)·2001
Exclusion of growth factor gene mutations as a common cause of Sotos syndrome.
American journal of medical genetics·2001
Sudden death in childhood due to right ventricular dysplasia: report of two cases.
Pediatric pathology·1994
Organ weights in sudden infant death syndrome.
Pediatric pathology·1994
Giant cell and lymphocytic interstitial pneumonia associated with fetal pneumonia.
Pediatric pathology·1994
Autoimmune-Like Hepatitis Triggered by Methylprednisolone: A Case Report about the Paradox of Treating DILI with the Offending Drug.
GE Portuguese journal of gastroenterology·2026
Duodenal Strongyloidiasis Mimicking Inflammatory Bowel Disease: A Case Report of a 52-Year-Old Immunocompetent Woman.
Clinical medicine insights. Case reports·2026
Bilateral IgG4-Related Dacryoadenitis.
Clinical case reports·2026
Giant chronic splenic infarction mimicking splenic neoplasm in a patient with rheumatic heart disease: a case report.
Frontiers in cardiovascular medicine·2026
Diagnostic methods of rheumatoid arthritis-associated interstitial lung disease: a systematic review.
Rheumatology international·2026