ABSTRACT Marden–Walker syndrome (MWS; OMIM 248700) is an extremely rare congenital disorder characterized by multiple joint contractures, craniofacial dysmorphism, neurological abnormalities, and multisystem involvement. Although historically diagnosed on clinical grounds, only a few cases have been molecularly confirmed.
Guilherme Sotto Battiston +35 more
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A Rare Familial Case of Harlequin Ichthyosis in an Infant of a Diabetic Mother: A Diagnostic and Management Challenge in Low and Middle Income Settings. [PDF]
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Application of a modified lung ultrasound score in assessing the severity of neonatal pneumonia: a multicenter prospective study. [PDF]
Cheng J, Ge H, Huang Y.
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Influence of volume conductor model errors on EEG dipole source localization in neonates
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Clinical Trials of Fetal Therapy With Continuing Neonatal Interventions: Legal Requirements and Customary Procedures Regarding Parental Consent. The BOOSTB4 Trial as a Case Study. [PDF]
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Contribution of maternal gut carriage to neonatal acquisition of extended-spectrum beta-lactamase-producing Enterobacterales in Madagascar and Cambodia. [PDF]
Beaumont AL +18 more
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Congenital scoliosis with truncus arteriosus type 1 in a preterm neonate: A case report. [PDF]
Omullo P +4 more
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