Related Experiment Videos
Noonan's syndrome and neurofibromatosis
Archives of Disease in Childhood
|February 1, 1987
Abstract:
A child with Noonan syndrome and multiple cafe au lait spots, compatible in size and number with von Recklinghausen's neurofibromatosis, is presented. These features may represent a distinct genetic entity rather than the coincidence of two diseases.
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Role of artificial intelligence, machine learning and deep learning models in corneal disorders - A narrative review.
Journal francais d'ophtalmologie·2024
[Endometriosis: Assessment of the Ultrasound-Based Endometriosis Staging System score (UBESS) in predicting surgical difficulty].
Gynecologie, obstetrique, fertilite & senologie·2019
Precaval positive sentinel lymph node with bilateral negative pelvic sentinel lymph node in low-risk endometrial cancer patient.
Journal of gynecology obstetrics and human reproduction·2018
What about sentinel lymph node biopsy for early breast cancer during pregnancy?
Journal of gynecology obstetrics and human reproduction·2018
Evaluation of adherence to French clinical practice guidelines in the management of pregnancy loss issued by the French College of Obstetricians and Gynecologists, one year after publication: A vignette-based study.
Journal of gynecology obstetrics and human reproduction·2017
Impacts of vaping on children and young people: a systematic review.
Archives of disease in childhood·2026
Informed, autonomous and safe: a qualitative study describing the views of English adolescents on consent to participate in medical research.
Archives of disease in childhood·2026
National variations within the timings of transport to paediatric intensive care from 2018 to 2022: a cohort study.
Archives of disease in childhood·2026
Using directed acyclic graphs in observational research: a practical guide for paediatric researchers.
Archives of disease in childhood·2026
Trends in neonatal mortality and morbidity at a tertiary centre over four decades: a cohort study.
Archives of disease in childhood·2026
A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.
American journal of medical genetics. Part A·2026
Whole-genome and pan-genome analyses reveal genomic differences among nontypeable Haemophilus influenzae isolates from bronchiectasis, community-acquired pneumonia, and chronic obstructive pulmonary disease.
Frontiers in cellular and infection microbiology·2026
CLUAP1 variants cause non-syndromic retinitis pigmentosa.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie·2026