• <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
• Acquired cutis laxa: a clinical review
• 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