• "SITUS INVERSUS VISCERUM" FROM THE POINT OF VIEW OF ITS ANATOMICAL EXPRESSIONS AND FORMAL GENESIS (BASED ON 7 PERSONAL CASES)
• 3 INTERESTING CASES OF SITUS INVERSUS VISCERUM
• A case of appendicitis in situs inversus viscerum totalis
• A case of situs inversus viscerum
• A case of situs inversus viscerum completus
• A case of situs inversus viscerum; clinico-mechanical study of the cardiovascular system, with special reference to ballistocardiography
• A Case Report of Dextrocardia with Situs Inversus: A Rare Condition and Its Clinical Importance
• A mouse model of conduction system patterning abnormalities in heterotaxy syndrome
• A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect
• A pediatric case of primary ciliary dyskinesia caused by novel copy number variation in PIH1D3
• Acute Cholecystitis in a Patient With Situs Inversus
• An unusual case of heterotaxy and polysplenia syndrome associated with hemiazygous continuation of the left-sided vena cava inferior, dilated azygous vein and large venous ectasia
• Apparent X-linked primary ciliary dyskinesia associated with retinitis pigmentosa and a hearing loss
• Ballistocardiogram of patients with subacute rheumocarditis with situs inversus viscerum
• CANCER OF THE STOMACH IN A PATIENT WITH TOTAL VISCERAL SITUS INVERSUS
• Cardiac surgery for annuloaortic ectasia and mitral regurgitation in an adult patient with dextrocardia
• Case of dextrocardia with situs inversus viscerum
• Case of parathyroid osteosis associated with situs inversus viscerum
• Cavopulmonary pathway modification in patients with heterotaxy and newly diagnosed or persistent pulmonary arteriovenous malformations after a modified Fontan operation
• Clinical and genetic analysis of a family with Joubert syndrome type 10 caused by OFD1 gene mutation
• Clinical aspects of defects in the determination of laterality
• Clinical care of children with primary ciliary dyskinesia
• Common mesentery in situs inversus viscerum
• Complete situs inversus viscerum with congenital heart failure & the Klippel-Feil syndrome
• Complete situs inversus viscerum with congenital heart failure & the Klippel-Feil syndrome
• Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects
• Craniorachischisis and heterotaxia with heart disease in twins: link or change nature?
• Dexiocardia with situs inversus viscerum and congenital atrioventricular block
• Dextrocardia with situs inversus associated with non-compaction cardiomyopathy
• Dextroversion and noncompaction
• Disturbance of morphological laterality in humans
• Diverticulum of the stomach in a patient with complete situs inversus viscerum
• DNAI1 mutations explain only 2% of primary ciliary dykinesia
• Echinococcosis of the gallbladder with kidney disease in a case of complete situs inversus viscerum
• Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genes
• Experience with bidirectional cavopulmonary anastomosis and modified Fontan operation in patients with single ventricle and concomitant visceral heterotaxy
• Experimental twinning and situs inversus viscerum in the bird embryo
• Familial heterotaxy syndrome. Case report and review of the international literature
• FOXJ1 Variants Causing Primary Ciliary Dyskinesia with Hydrocephalus: A Case Report from Japan
• Fundus findings and longitudinal study of visual acuity loss in patients with X-linked retinoschisis
• GASTRIC CANCER WITH COMPLETE VISCERAL SITUS INVERSUS
• Genetics of human left-right axis malformations
• Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants
• Heterotaxia syndrome and autosomal dominant inheritance
• Heterotaxy syndrome: defining contemporary disease trends
• Heterotaxy syndrome: implications for anesthesia management
• Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects
• Identification of a frame shift mutation in the CCDC151 gene in a Han-Chinese family with Kartagener syndrome
• Identification of a novel ZIC3 isoform and mutation screening in patients with heterotaxy and congenital heart disease
• Increased postoperative and respiratory complications in patients with congenital heart disease associated with heterotaxy
• Intracardiac Fontan procedure for heterotaxy syndrome with complex systemic and pulmonary venous anomalies
• Isolated laevocardia with situs inversus viscerum
• Laparoscopic sleeve gastrectomy in a patient with situs inversus totalis: A case report
• Malformations associated with cystic disease of the lung and bronchiectasis with special reference to situs inversus viscerum; two clinical cases: association with congenital heart disease and Kartagener's syndrome
• Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1
• Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesia
• ON SITUS INVERSUS VISCERUM AND ASSOCIATED CONGENITAL ANOMALIES
• ON VARIOUS CASES OF ANOMALIES OF POSITION OF THE HEART WITH AND WITHOUT SITUS INVERSUS VISCERUM
• PAGOD syndrome and vascular anomalies: is a defect embryonic angiogenesis? A case report and review
• PCD and RP: X-linked inheritance of both disorders?
• Percutaneous closure of atrial septal defect with situs solitus and dextrocardia
• PIH1D3-knockout rats exhibit full ciliopathy features and dysfunctional pre-assembly and loading of dynein arms in motile cilia
• Polysplenia and situs inversus in siblings. Case reports
• Practical diagnostic features and clinical implications of situs inversus viscerum totalis
• Primary ciliary dyskinesia diagnosed on nasal mucosal biopsy in two newborns
• Primary ciliary dyskinesia: clinical presentation, diagnosis and genetics
• Rare novel variants in the ZIC3 gene cause X-linked heterotaxy
• Reply: To PMID 24030083
• Resection of the stomach in situs inversus viscerum
• Role of four-dimensional ultrasound (spatiotemporal image correlation and sonography-based automated volume count) in prenatal assessment of atrial morphology in cardiosplenic syndromes
• RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa
• RPGR mutations might cause reduced orientation of respiratory cilia
• Severe COVID-19 acute respiratory distress syndrome in an adult with single-ventricle physiology: a case report
• Sinusitis, otitis media and diffuse bronchiectasis in both lungs
• Situs ambiguus in a female fetus with balanced (X;21) translocation--evidence for functional nullisomy of the ZIC3 gene?
• Situs inversus totalis and a novel ZIC3 mutation in a family with X-linked heterotaxy
• Situs inversus totalis viscerum; considerations of a case
• Situs inversus viscerum
• Situs inversus viscerum
• Situs inversus viscerum and bronchiectasis; report of a Bantu case associated with chronic cor pulmonale and renal anomalies
• Situs inversus viscerum in a white rat (Mus norvegicus)
• Situs inversus viscerum in conjoined twins of the brook trout
• Situs inversus viscerum, bronchiectasis and sinusitis: three cases of Kartagener syndrome
• Situs inversus viscerum; observations in a mental patient; relations between visceral heterotaxia & nervous system
• Situs inversus viscerum; observations in a mental patient; relations between visceral heterotaxia & nervous system
• Skewed X-chromosome inactivation drives the proportion of <em>DNAAF6</em>-defective airway motile cilia and variable expressivity in primary ciliary dyskinesia
• Spontaneous gastric perforation in a child with heterotaxy syndrome
• Syndrome of dextroversion of the heart associated with splenic agenesis and partial visceral heterotaxia
• Truncating mutations in exons 20 and 21 of <em>OFD1</em> can cause primary ciliary dyskinesia without associated syndromic symptoms
• Twins with situs inversus viscerum in a trout embryo
• Two rights make a wrong: human left-right malformations
• Two-stent telescoping technique for securing an atrially embolized venous stent
• Unusual inheritance of primary ciliary dyskinesia (Kartagener's syndrome)
• Visceral heterotaxy in the developing world
• X-linked laterality sequence in a family with carrier manifestations
• X-linked laterality sequence: situs inversus, complex cardiac defects, splenic defects
• X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3
• X-linked situs abnormalities result from mutations in ZIC3
• ZIC3 in Heterotaxy
• Zic3 is required in the migrating primitive streak for node morphogenesis and left-right patterning