Search Results - "Kapur, Raj"

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  1. 1

    Histology of the Transition Zone in Hirschsprung Disease by Kapur, Raj P

    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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    Journal Article
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    Histopathological, Ultrastructural, and Immunohistochemical Findings in MYH11-Variant Visceral Myopathy by Kapur, Raj P.

    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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  3. 3

    Expression of Calretinin in the Cecal Muscularis Interna: Observation and Hypothetical Relevance to Appendicitis by Kapur, Raj P.

    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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  4. 4

    Diagnosis of Hirschsprung Disease by Ambartsumyan, Lusine, Smith, Caitlin, Kapur, Raj P

    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 by Kapur, Raj P.

    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 by Smith, Caitlin, Ambartsumyan, Lusine, Kapur, Raj P

    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 by Kapur, Raj P, Reyes-Mugica, Miguel

    “…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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    Postoperative Pullthrough Obstruction in Hirschsprung Disease: Etiologies and Diagnosis by Kapur, Raj P, Smith, Caitlin, Ambartsumyan, Lusine

    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. 10

    Complex I deficiency due to loss of Ndufs4 in the brain results in progressive encephalopathy resembling Leigh syndrome by Quintana, Albert, Kruse, Shane E., Kapur, Raj P., Sanz, Elisenda, Palmiter, Richard D.

    “…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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  11. 11

    Calretinin-Immunoreactive Mucosal Innervation in Very Short-Segment Hirschsprung Disease: A Potentially Misleading Observation by Kapur, Raj P.

    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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  12. 12

    A new approach for automation of location-based earthwork scheduling in road construction projects by Shah, Raj Kapur

    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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    Practical pathology and genetics of Hirschsprung's disease by Kapur, Raj P., MD, PhD

    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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  15. 15

    Are We Underdiagnosing Hirschsprung Disease? by Kapur, Raj P, Ambartsumyan, Lusine, Smith, Caitlin

    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 by Gacem, Nadjet, Kavo, Anthula, Zerad, Lisa, Richard, Laurence, Mathis, Stephane, Kapur, Raj P., Parisot, Melanie, Amiel, Jeanne, Dufour, Sylvie, de la Grange, Pierre, Pingault, Veronique, Vallat, Jean Michel, Bondurand, Nadege

    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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  17. 17

    Myelin Protein Zero Immunohistochemistry Is Not a Reliable Marker of Extrinsic Mucosal Innervation in Patients With Hirschsprung Disease by Kapur, Raj P., Tisoncik-Go, Jennifer, Gale, Michael

    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 by Green, Nicole, Smith, Caitlin A., Bradford, Miranda C., Ambartsumyan, Lusine, Kapur, Raj P.

    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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    Mice with Mitochondrial Complex I Deficiency Develop a Fatal Encephalomyopathy by Kruse, Shane E., Watt, William C., Marcinek, David J., Kapur, Raj P., Schenkman, Kenneth A., Palmiter, Richard D.

    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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