Suman Ghosh

Dravet Syndrome Associated With a CSNK2B-Related Neurodevelopmental Disorder

Abena O Yeboaha, Charles Tyshkov, Suman Ghosh

Dravet syndrome (DS) is a developmental epileptic encephalopathy characterized by prolonged febrile and afebrile focal clonic as well as generalized seizures. The most common genetic etiology is SCN1A, but other genetic disorders can present with the phenotype. A two-year-and-11-month-old Caucasian female patient …

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EGFR Expression and its Association with Molecular Subtypes of Breast Carcinoma: A Cross-sectional Study

Anisa Barman, Suman Ghosh, Subhasish Bandyopadhyay, Anadi Roy Chowdhury

Introduction: The incidence of breast carcinoma is rising worldwide. The Epidermal Growth Factor Receptor (EGFR) is a tyrosine kinase receptor that serves as an independent prognostic marker of poor clinical outcomes and aggressiveness in breast carcinoma. EGFR overexpression is specific to Triple-Negative …

Chronic Wound Healing

A T. Patel, Priyanti Halder, Jayshree Manahty, Radheshyam Pal et autres

Chronic wounds are signified as a silent global epidemiological outbreak on account of rising incidences. According to the body�s innate response to injury, the process of wound healing is immediately initiated, but sometimes the wounds appear as chronic with delayed impaired healing …

A critical review on SGLT2 inhibitors for diabetes mellitus, renal health, and cardiovascular conditions

Nitish Kumar, Bimlesh Kumar, Sumel Ashique, Sabina Yasmin et autres

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Helicobacter Pylori and Metaplastic Changes in Chronic Cholecystitis: A Correlation Study

Rabiul Alam, Swapan Kumar Sarkar, Subhasish Bandyopadhyay, S. Chakrabarti et autres

Abstract Introduction : Various types of metaplastic changes, such as gastric metaplasia (foveolar type or antral type) and intestinal metaplasia, are observed in chronic cholecystitis but not in normal mucosa. Helicobacter species can be detected in the bile and gallbladder tissue of …

Hereditary sensory autonomic neuropathy type VI in the age of genetic testing

Lekshmi Peringassery Sateesh, Pavani Chitamanni, Danielle Akinsanmi, Suman Ghosh et autres

Abstract Background Hereditary sensory and autonomic neuropathy type VI (HSAN VI) is a rare recessive genetic disorder caused by mutations in the human dystonin (DST) gene. We report a novel homozygous alternate transcript mutation in the DST gene causing a severe neonatal …

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Prevalence and Risk Factors for Cerebral Palsy in Children With Congenital Heart Disease Based on Risk of Surgical Mortality

Suman Ghosh, Ing Grace Lien, Kerstin Martinez, Tracy Lin et autres

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Using interleukin-18, Eotaxin-1, and Eotaxin-3 to identify brain injury in neonates with congenital heart disease

Suman Ghosh, Mark S. Bleiweis, Jeffrey P. Jacobs, Eduardo Candelario‐Jalil

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Association Between Urinary Biomarkers and CKD in Extremely Low Gestational Age Neonates

Sangeeta Hingorani, Robert H. Schmicker, Brian Halloran, Patrick D. Brophy et autres

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Prognostic and Diagnostic Utility of Serum Biomarkers in Pediatric Traumatic Brain Injury

Jennifer C. Muñoz Pareja, Juan Pablo de Rivero Vaccari, Maria Mateo Chavez, Maria Kerrigan et autres

Traumatic brain injury (TBI) remains a major cause of morbidity and death among the pediatric population. Timely diagnosis, however, remains a complex task because of the lack of standardized methods that permit its accurate identification. The aim of this study was to …

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Noninvasive Neuromonitoring Modalities in Children Part I: Pupillometry, Near-Infrared Spectroscopy, and Transcranial Doppler Ultrasonography

Marlina E. Lovett, Jennifer M. MacDonald, Marina Villalón Mir, Suman Ghosh et autres

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Combined GFAP, NFL, Tau, and UCH-L1 panel increases prediction of outcomes in neonatal encephalopathy

Zhihui Yang, Haiyan Xu, Livia Sura, Rawad Daniel Arja et autres

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