Search Results - "Kapur, Raj"
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Histology of the Transition Zone in Hirschsprung Disease
Published in The American journal of surgical pathology (01-12-2016)“…Surgical management of Hirschsprung disease requires resection of the aganglionic bowel and transition zone, a length of ganglionic bowel, immediately proximal…”
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Histopathological, Ultrastructural, and Immunohistochemical Findings in MYH11-Variant Visceral Myopathy
Published in Pediatric and developmental pathology (01-01-2023)“…Background: Pathogenic mutations in the smooth muscle myosin heavy chain gene, MYH11, cause megacystis megacolon intestinal hypoperistalsis syndrome and other…”
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Expression of Calretinin in the Cecal Muscularis Interna: Observation and Hypothetical Relevance to Appendicitis
Published in Pediatric and developmental pathology (01-05-2024)“…Background: The unexpected observation of calretinin immunoreactivity in smooth muscle cells in the muscularis propria of the cecum led to a more detailed…”
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Diagnosis of Hirschsprung Disease
Published in Pediatric and developmental pathology (01-01-2020)“…Diagnosis or exclusion of Hirschsprung disease (HSCR) is a frequent exercise in any pediatric hospital. Although HSCR may present at different ages and with…”
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Submucosal nerve diameter of greater than 40 μm is not a valid diagnostic index of transition zone pull-through
Published in Journal of pediatric surgery (01-10-2016)“…Submucosal nerve hypertrophy is a feature of the transition zone in Hirschsprung disease and has been used as a primary diagnostic feature of transition zone…”
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Surgery, Surgical Pathology, and Postoperative Management of Patients With Hirschsprung Disease
Published in Pediatric and developmental pathology (01-01-2020)“…Endorectal pullthrough surgery is integral in the treatment of patients with Hirschsprung disease. Several different surgical procedures exist, which share as…”
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Intestinal Neuronal Dysplasia Type B: An Updated Review of a Problematic Diagnosis
Published in Archives of pathology & laboratory medicine (1976) (01-02-2019)“…Intestinal neuronal dysplasia type B (IND B) is a controversial histopathologic phenotype that has been associated with intestinal dysmotility, either as an…”
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Adult enteric nervous system in health is maintained by a dynamic balance between neuronal apoptosis and neurogenesis
Published in Proceedings of the National Academy of Sciences - PNAS (02-05-2017)“…According to current dogma, there is little or no ongoing neurogenesis in the fully developed adult enteric nervous system. This lack of neurogenesis leaves…”
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Postoperative Pullthrough Obstruction in Hirschsprung Disease: Etiologies and Diagnosis
Published in Pediatric and developmental pathology (01-01-2020)“…Some patients continue to have obstructive symptoms and/or incontinence after pullthrough surgery for Hirschsprung disease. Incontinence can be due to injury…”
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10
Complex I deficiency due to loss of Ndufs4 in the brain results in progressive encephalopathy resembling Leigh syndrome
Published in Proceedings of the National Academy of Sciences - PNAS (15-06-2010)“…To explore the lethal, ataxic phenotype of complex I deficiency in Ndufs4 knockout (KO) mice, we inactivated Ndufs4 selectively in neurons and glia (NesKO…”
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Calretinin-Immunoreactive Mucosal Innervation in Very Short-Segment Hirschsprung Disease: A Potentially Misleading Observation
Published in Pediatric and developmental pathology (01-01-2014)“…Absent calretinin-immunoreactive (CRir) mucosal innervation in aganglionic rectal biopsies is considered a useful diagnostic finding for Hirschsprung disease…”
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A new approach for automation of location-based earthwork scheduling in road construction projects
Published in Automation in construction (01-07-2014)“…Accurate information of working locations is vital for efficient resource planning, safety of the construction site and monitoring the weekly progress of…”
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13
Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primate
Published in Nature medicine (01-11-2016)“…New animal models of Zika virus (ZIKV) infection are imperative to accelerating efforts to treat or prevent disease in humans. Adams Waldorf et al . now report…”
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Practical pathology and genetics of Hirschsprung's disease
Published in Seminars in pediatric surgery (01-11-2009)“…Diagnosis and management of Hirschsprung's disease (HSCR) requires understanding of the malformation's anatomic features and multigenic nature. Rectal…”
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Are We Underdiagnosing Hirschsprung Disease?
Published in Pediatric and developmental pathology (01-01-2020)“…Hirschsprung disease (HSCR) is conventionally defined as aganglionosis of the distal rectum and a variable length of proximal contiguous bowel with a…”
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ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development
Published in Nature communications (10-01-2020)“…The neural crest gives rise to numerous cell types, dysfunction of which contributes to many disorders. Here, we report that adenosine deaminase acting on RNA…”
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Myelin Protein Zero Immunohistochemistry Is Not a Reliable Marker of Extrinsic Mucosal Innervation in Patients With Hirschsprung Disease
Published in Pediatric and developmental pathology (01-07-2022)“…Background Innervation of aganglionic rectum in Hirschsprung disease derives from extrinsic nerves which project from cell bodies located outside the bowel…”
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Rectal suction biopsy versus incisional rectal biopsy in the diagnosis of Hirschsprung disease
Published in Pediatric surgery international (01-12-2022)“…Background Hirschsprung disease is one of the most common congenital anomalies that affect colorectal function. Rectal biopsy demonstrating the absence of…”
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Disruption of myelin structure and oligodendrocyte maturation in a macaque model of congenital Zika infection
Published in Nature communications (18-06-2024)“…Zika virus (ZikV) infection during pregnancy can cause congenital Zika syndrome (CZS) and neurodevelopmental delay in infants, of which the pathogenesis…”
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Mice with Mitochondrial Complex I Deficiency Develop a Fatal Encephalomyopathy
Published in Cell metabolism (01-04-2008)“…To study effects of mitochondrial complex I (CI, NADH:ubiquinone oxidoreductase) deficiency, we inactivated the Ndufs4 gene, which encodes an 18 kDa subunit of…”
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