• A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease
• Alice Vance ("Das Barenweib"): a historical case of Nievergelt syndrome
• Association between traumatic brain injury and risk of posttraumatic stress disorder in active-duty Marines
• Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles
• Concomitant rhomboid-shaped tibiae and fibulae, finger-like projections, and orthopedic management in a new variant of nievergelt syndrome: A case report
• Delayed sleep phase syndrome is related to seasonal affective disorder
• Disruption of vascular homeostasis in patients with Kawasaki disease: involvement of vascular endothelial growth factor and angiopoietins
• Double bilateral talocalcaneal and calcaneonavicular coalition in a 15 year-old patient: treatment and results
• Familial mesomelial dwarfism (Nievergelt syndrome)
• FAMILIAL TARSAL AND CARPAL SYNOSTOSIS WITH RADIAL-HEAD SUBLUXATION (NIEVERGELT'S SYNDROME)
• FMR1, circadian genes and depression: suggestive associations or false discovery?
• Genetic variants associated with sleep disorders
• Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders
• Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndrome
• Letter to the Editor: Posttraumatic stress disorder has genetic overlap with cardiometabolic traits
• Longitudinal epiphyseal bracket
• Longitudinal tibial epiphyseal bracket in Nievergelt syndrome
• Matrix metalloproteinase haplotypes associated with coronary artery aneurysm formation in patients with Kawasaki disease
• Mesomelic dysplasia with absence of fibulae and hexadactyly: Nievergelt syndrome or new syndrome?
• Neglected Bilateral Clubfoot Clubhand Deformity
• Nievergelt syndrome
• Nievergelt syndrome (mesomelic dwarfism-type Nievergelt)
• Nievergelt syndrome and its treatment: a case report
• Nievergelt-Pearlman syndrome with impairment of hearing. Report of three cases in a family
• Nievergelt-Pearlman syndrome. Synostosis in feet and hands with dysplasia of elbows. Report of a case
• Nievergelt's syndrome and bilateral temporomandibular ankylosis
• Patient with the mesomelic dysplasia, Nievergelt syndrome, and cerebellovermian agenesis and cataracts
• Peptide YY (PYY) gene polymorphisms in the 3'-untranslated and proximal promoter regions regulate cellular gene expression and PYY secretion and metabolic syndrome traits in vivo
• Peptide YY (PYY) Gene Polymorphisms in the 3'-Untranslated Region and Proximal Promoter Regions Regulate Cellular Gene Expression and PYY Secretion and Metabolic Syndrome Traits in Vivo
• Prevalence of suicidal ideation and other suicide warning signs in veterans attending an urgent care psychiatric clinic
• Rare copy number variation in posttraumatic stress disorder
• Rhomboid shaped tibia and hypoplastic fibula: a variant of Nievergelt syndrome
• Severe limb abnormalities: Nievergelt or new syndrome?
• Surgical Considerations for Massive Tarsal Coalitions in Multiple Synostosis Syndrome: A Case Report
• Symphalangism with metacarpophalangeal fusions and elbow abnormalities
• Temporomandibular ankylosis and Nievergelt's syndrome
• The multiple synostoses syndrome. A plea for simplicity
• Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4
• Ulno-fibular dysplasia. An autosome-dominant hereditary micromesomelia resembling the Nievergelt syndrome
• Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy