• A Novel COL2A1 Gene Pathogenic Variant in a Turkish Family With Ocular Stickler Syndrome
• A patient with concurrent Axenfeld-Rieger and Stickler syndromes verified by molecular genetics
• Anesthetic Consideration in Pierre Robin Sequence
• Anesthetic Consideration in Pierre Robin Sequence
• Anesthetic Management of a Cesarean Section for Preeclampsia in a Parturient With Stickler Syndrome: A Case Report
• Associated anomalies in Pierre Robin sequence
• Axial length shortening in myopic children with Stickler syndrome after repeated low-level red-light therapy
• Cambridge Prophylactic Protocol, Retinal Detachment, and Stickler Syndrome
• Case report: Autosomal recessive type 3 Stickler syndrome caused by compound heterozygous mutations in <em>COL11A2</em>
• Characteristics of a Three-Generation Family with Stickler Syndrome Type I Carrying Two Different COL2A1 Mutations
• Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia
• Clinician Awareness of Stickler Syndromes Among Australian Allied Health Care Professionals
• Developmental outcome of children with Robin sequence treated with the current Paris protocol
• Effects of tributyrin supplementation on ruminal microbial protein yield, fermentation characteristics and nutrients degradability in adult Small Tail ewes
• Epidemiology of Robin sequence in the UK and Ireland: an active surveillance study
• Establishment and characterization of SUIT-58 pancreas cancer cell line and its subline S58-SF adapted to serum-free condition derived from metastatic liver tumor
• Exome sequencing-aided precise diagnosis of four families with type I Stickler syndrome
• Features of genetic mutations in children with high myopia combined with peripheral retinal degenerations
• Identification and functional characteristics of a novel splicing heterozygote variant of COL2A1 associated with Stickler syndrome type I
• Knobloch syndrome - a rare collagenopathy, revealing peripheral avascular retina
• Management of an Anticipated Difficult Airway in a Pediatric Patient With Stickler Syndrome
• Microphthalmia and congenital cataract in two patients with Stickler syndrome type II: a case report
• Multidisciplinary approach to inherited causes of dual sensory impairment
• Multiocular defect in the Old English Sheepdog: A canine form of Stickler syndrome type II associated with a missense variant in the collagen-type gene COL11A1
• Nonperfusion of the Far Peripheral Retina in Highly Myopic Stickler Syndrome
• Novel LOXL3-associated stickler syndrome-like phenotype: a case report
• Ophthalmic manifestations of Czech dysplasia
• Outcomes in Retinal Detachment Repair and Laser Prophylaxis for Syndromes with Optically Empty Vitreous
• Outcomes of rhegmatogenous retinal detachment surgery in patients with Stickler syndrome
• Pattern of choroidal thickness in early-onset high myopia
• Peripapillary Hyper-Reflective Ovoid Mass-like Structures in Stickler syndrome
• Peripapillary Hyperreflective Ovoid Mass-Like Structures in Stickler Syndrome
• Posterior Precortical Vitreous Pocket in Stickler Syndrome: A Report of Two Cases
• Preventing Retinal Detachment: The Encircling Laser Retinopexy Technique
• Recurrent Retinal Detachment in Stickler Syndrome
• Reponse to letter to editor regarding our recently published paper "Laser Prophylaxis in Stickler Syndrome: The Manchester Protocol"
• Response to letter to editor regarding our recently published paper "Laser Prophylaxis in Stickler Syndrome: The Manchester Protocol"
• Retinal detachment with multiple macrocysts in Stickler syndrome: case report and review of the literature
• Spontaneously reattached bilateral retinal detachment in Stickler syndrome
• Stickler Syndrome
• Streptococcal pyomyositis in asplenia and underlying connective tissue disease
• Sub-toxic concentrations of nano-ZnO and nano-TiO₂ suppress neurite outgrowth in differentiated PC12 cells
• Surgical outcome and treatment trends in 1289 infants with micrognathia: a multicenter cohort
• Syndromic Piere Robbin Sequence- A Rare Presentation in Association with Multiple Heart Defects and Type III Stickler Syndrome
• The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High Myopia
• The molecular complexity of COL2A1 splicing variants and their significance in phenotype severity
• Unraveling the genetic collagen connection: clinical and therapeutic insights on genetic connective tissue disorders
• Use of vitreous phenotype as a key clinical marker to identify Ocular-only Stickler syndrome in a family with Marfan syndrome
• Utilization of Anti-obesity Medications After Bariatric Surgery: Analysis of a Large National Database
• Vitreopapillary Traction in Stickler Type IV COL9A1
• Vitreoretinopathy-Associated Pediatric Retinal Detachment Treatment Outcomes: IRIS® Registry (Intelligent Research in Sight) Analysis