Disease: Marshall syndrome
- <em>Col11a1a</em> Expression Is Required for Zebrafish Development
- A case of Marshall's syndrome (postinflammatory elastolysis)
- A novel mutation in the COL2A1 gene in a patient with Stickler syndrome type 1: a case report and review of the literature
- A PSD-95 peptidomimetic mitigates neurological deficits in a mouse model of Angelman syndrome
- A Very Rare Case of Diabetes Mellitus Occurring in a Patient With Hyperinsulinism Hyperammonemia Syndrome
- Abnormalities in Clostridioides and related metabolites before ACTH treatment may be associated with its efficacy in patients with infantile epileptic spasm syndrome
- Acquired cutis laxa secondary to Sweet syndrome in a child (Marshall syndrome): A rare case report
- Acquired cutis laxa type II (Marshall syndrome) in a 3-month-old boy
- Audiologic Manifestations of Marshall Syndrome
- Congenital keratoglobus with blue sclera in two siblings with overlapping Marshall/Stickler phenotype
- Considerations for patient and public involvement and engagement in health research
- Distinct host-response signatures in circulatory shock: a narrative review
- Distinguishing Marshall from Stickler syndrome: a clinical and genetic challenge
- Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study
- Expanding the phenotype spectrum associated with pathogenic variants in the COL2A1 and COL11A1 genes
- Features of genetic mutations in children with high myopia combined with peripheral retinal degenerations
- Growing up with Marshall syndrome: A case report from infancy to age 12.5 years
- Is colchicine an effective treatment in periodic fever, aphtous stomatitis, pharyngitis, cervical adenitis (PFAPA) syndrome?
- Leigh syndrome: an adult presentation of a paediatric disease
- Marshall and stickler syndrome in one family
- Marshall syndrome
- Marshall syndrome in a young child, a reality: Case report
- Modulating the immune system as a therapeutic target for myelodysplastic syndromes and acute myeloid leukemia
- Monoclonal Antibody Therapy of Breastfeeding Patient Infected with SARS-CoV-2: A Case Report
- Outcomes and characteristics of patients hospitalized for COVID-19 in British Columbia, Ontario and Quebec during the Omicron wave
- PFAPA syndrome in children
- Predictors and Outcomes of Extracorporeal Membrane Oxygenation in COVID-19 Patients With ARDS: A Propensity-Matched Analysis of National Inpatient Sample
- Prenatal Intravenous Magnesium at 30-34 Weeks' Gestation and Neurodevelopmental Outcomes in Offspring: The MAGENTA Randomized Clinical Trial
- Spectrum of auto-inflammatory diseases in Morocco: a monocentric experience
- SSSH: ReSponsive Soothing bassinet feasibility Study for infants with congenital Heart disease after cardiac surgery
- Structure-based development of new cyclic compounds targeting PSD-95 PDZ3 domain
- Sweet syndrome of childhood with acquired cutis laxa (Marshall syndrome) as primary manifestation of Takayasu arteritis
- Symptom-led staging for semantic and non-fluent/agrammatic variants of primary progressive aphasia
- The Modified Clinical Progression Scale for Pediatric Patients: Evaluation as a Severity Metric and Outcome Measure in Severe Acute Viral Respiratory Illness
- The Shape of the Jaw-Zebrafish Col11a1a Regulates Meckel's Cartilage Morphogenesis and Mineralization