A5005457042- Glioma Diagnosis and Treatment
- Kawasaki Disease and Coronary Complications
- COVID-19 Clinical Research Studies
- Hedgehog Signaling Pathway Studies
- Autoimmune and Inflammatory Disorders Research
- Venous Thromboembolism Diagnosis and Management
- Cardiovascular Issues in Pregnancy
- Vitamin K Research Studies
- Sarcoma Diagnosis and Treatment
- Blood Coagulation and Thrombosis Mechanisms
- Chromatin Remodeling and Cancer
- COVID-19 and healthcare impacts
- Lymphoma Diagnosis and Treatment
- Adolescent and Pediatric Healthcare
- Bone Tumor Diagnosis and Treatments
- Cardiovascular Syncope and Autonomic Disorders
- Cardiovascular Disease and Adiposity
- Coronary Artery Anomalies
- Pharmacological Effects and Toxicity Studies
- Cardiac Arrhythmias and Treatments
- CNS Lymphoma Diagnosis and Treatment
- Antibiotics Pharmacokinetics and Efficacy
- Coagulation, Bradykinin, Polyphosphates, and Angioedema
- Metabolism and Genetic Disorders
- Cardiac tumors and thrombi
Sinai Grace Hospital
2024
Detroit Medical Center
2024
Universal College of Medical Sciences
2020-2021
Patan Academy of Health Sciences
2021
B.P. Koirala Institute of Health Sciences
2021
Universal College
2020-2021
College of Medical Sciences
2020-2021
SUNY Upstate Medical University
2020-2021
Nidan
2020-2021
Guthrie Robert Packer Hospital
2020-2021
MPL (myxoid pleomorphic liposarcoma) is an uncommon type of liposarcoma that affects mostly children and infants. Its aggressive behavior tendency to recur warrant complete excision despite the challenges troublesome locations.A 12-month-old infant presented with insidious onset noisy breathing respiratory distress not relieved by supplemental oxygen via face mask. Examination revealed dullness decreased air entry on left chest. Computed Tomographic (CT) scan showed a large solid mass...
Factor XI deficiency is a rare condition with an estimated prevalence of about one in million and more commonly seen Ashkenazi Jews (8-9%) due to consanguinity. It occurs because mutations the factor gene (F11) on chromosome 4(4q35). Patients this disorder may remain asymptomatic until they undergo any surgical procedure or delivery. The most common sites bleeding include oral cavity, pharynx, genitourinary tract, where there high fibrinolytic activity. Our patient was his whole life. He...
Coronavirus disease (COVID-19) is a global health crisis leading to increased morbidity and mortality worldwide. It associated with activation of the clotting system thrombotic complications increasing risk life-threatening complications. We report case 70-years-old COVID-19 positive patient who presented both lower extremities forearm pain. On workup, she was found have an extensive arterial clot. In patients COVID-19, clots may be initial presenting symptoms hospital can fatal if not...
Primary central nervous system lymphoma (PCNSL) is a rare form of CNS tumor. Immunosuppression the most important risk factor PCNSL, but few immunocompetent individuals are also affected. The common clinical feature PCNSL includes dizziness and ataxia. Our patient was 71-year-old female who presented with progressive ataxia, imbalance, for one year. A homogenous enhancing lesion found in magnetic resonance imaging (MRI) head. One month later, on follow-up MRI, significant increase tumor size...
Medulloblastoma (MB) is an aggressive malignant tumor of the posterior fossa CNS that mainly affects children younger than 15 years age. It uncommon in adult population compared to children. Any patient presenting with cerebellar mass must be evaluated brain tissue biopsy rule out MB. Our a 27-year-old female who presented sudden onset frontal headache and was diagnosed
Kawasaki disease (KD) is an acute rheumatological illness usually affecting children between six months and five years of age. It a vasculitis syndrome medium-sized vessels that has typical clinical characteristics such as fever, rash, cervical lymphadenopathy, conjunctivitis, mucosal changes. However, sometimes, it may present with the features shock when known (KDSS). The actual etiology this still unknown. primary treatment aspirin intravenous immunoglobulin (IVIG). most common serious...
Pure autonomic failure is a neurodegenerative disorder affecting the nervous system which clinically presents with orthostatic hypotension. It diagnosis of exclusion after detailed clinical examinations and relevant investigations. Here, we discuss case 68 years old male who had complaints multiple episodes loss consciousness on standing from sitting position for last 3 years. The was considered by revealing dysfunctions normal appropriate patient treated successfully midodrine,...
Macrophage activation syndrome is a rare but life threatening condition commonly associated with Systemic Juvenile Idiopathic Arthritis. Its clinical presentation includes fever, hepatosplenomegaly, hypertriglyceridemia, hypofibrinogenemia, hyperferritinemia and impaired liver enzymes. The symptoms are alarming yet non-specific often lead to delayed diagnosis. A 12 year male presented history of intermittent fever was started on antibiotics failed respond after several days hospital stay....