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Isolated Cranial Nerve 6 Palsy in 6 Patients With COVID-19 Infection

Greer, Christine E; Bhatt, Jaydeep M; Oliveira, Cristiano A; Dinkin, Marc J
PMID: 32941331
ISSN: 1536-5166
CID: 4683832

Taking a Strohl Through History: Putting Strohl Back in Guillain-Barre-Strohl Syndrome [Meeting Abstract]

Bondi, Steven; Carroll, Elizabeth; Bhatt, Jaydeep
ISI:000536058001309
ISSN: 0028-3878
CID: 4561192

Taking a Strohl Through History: Putting Strohl Back in Guillain-Barré-Strohl Syndrome

Bondi, Steven; Carroll, Elizabeth; Bhatt, Jaydeep
Guillain-Barré Syndrome is a popular eponym that comes from a 1916 paper by Drs. Guillain, Barré, and Strohl. These physicians described two soldiers in the French Sixth Army during World War I who developed acute progressive motor weakness. Although Drs. Guillain and Barré have continued to be included in the syndrome's eponym, Dr. Strohl has been forgotten despite having strongly contributed to the original paper. The reasons previously mentioned for Dr. Strohl's absence appear trivial in contemporary practice and thus, his name deserves to be reintroduced to Guillain-Barré-Strohl Syndrome.
PMID: 32804099
ISSN: 2214-3602
CID: 4578022

Xpert MTB/RIF Ultra for Detection of Mycobacterium tuberculosis in Cerebrospinal Fluid [Letter]

Chin, Jerome H; Musubire, Abdu K; Morgan, Nicole; Pellinen, Jacob; Grossman, Scott; Bhatt, Jaydeep M; Wadda, Vincent; Ssengooba, Willy
PMCID:6535608
PMID: 30944199
ISSN: 1098-660x
CID: 3980982

Hypertension-A Global Neurological Problem

Chin, Jerome H; Bhatt, Jaydeep M; Lloyd-Smith, Alexandra J
PMID: 28166320
ISSN: 2168-6157
CID: 2437342

The Epidemiology of Neuromuscular Diseases

Bhatt, Jaydeep M
Neuromuscular disorders as a group are linked by anatomy with significant differences in pathogenetic mechanisms, clinical expression, and time course of disease. Each neuromuscular disease is relatively uncommon, yet causes a significant burden of disease socioeconomically. Epidemiologic studies in different global regions have demonstrated certain neuromuscular diseases have increased incidence and prevalence rates over time. Understanding differences in global epidemiologic trends will aid clinical research and policies focused on prevention of disease. There is a critical need to understand the global impact of neuromuscular diseases using metrics currently established for communicable and noncommunicable diseases.
PMID: 27720006
ISSN: 1557-9875
CID: 2278182

Fragile X Tremor Ataxia Syndrome With Rapidly Progressive Myopathy

Nirenberg, Melissa J; Bhatt, Jaydeep M; Roda, Ricardo H
PMID: 26258737
ISSN: 2168-6157
CID: 1720952

Singultus as a sequelae of lateral medullary infarction: Rehabilitation perspective. A case report

Kim, Eric; Bhatt, Jaydep
Hiccups are a rare manifestation of Lateral Medullary Infarction (LMI). Strokes produce numerous complications, hiccup manifestations are limited in reviewing literatures. Diagnoses of LMIs have been documented predominately by use of MRIs. There have been attempts to make clinical with MRI correlations in patients with LMI, studies with a large number of patients are uncommon among subjects with this etiology. Previous literatures have attempted to investigate anatomical lesions in patients with LMI suffering from hiccups by using imaging. Initial signs are usually headache, vertigo, dizziness or gait ataxia, whereas sensory symptoms consisting of dysphagia, hoarseness and hiccups usually occurred in the latter aspect. Hiccups in LMI are not fully understood and has been insufficiently studied. We describe a case of a man in his sixties with a constant occipital headache lasting 12 days associated with nausea and vomiting prior to admission to acute hospital. There was no history of exposure to any prescription or recreational drugs prior to presentation. The day after admission, he presented with intractable hiccups. Treatment with chlorpromazine (Thorazine) was unsuccessful, hiccups improved after initiation of baclofen and physical therapy. This case suggests that physical therapy may be a valuable aspect for refractory hiccups in conjunction with pharmacological management
ORIGINAL:0006938
ISSN: 1427-9622
CID: 140415

Amyotrophic lateral sclerosis (ALS)

Chapter by: Bhatt JM; Mitsumoto H
in: Encyclopedia of neuroscience by Squire LR [Eds]
Berlin: Elsevier, 2010
pp. 363-368
ISBN: 0080450466
CID: 4995

Current clinical trials in amyotrophic lateral sclerosis

Bhatt, Jaydeep M; Gordon, Paul H
Amyotrophic lateral sclerosis is caused by selective degeneration of motor neurons in the brain and spinal cord. There are still no other effective therapies 10 years after the approval of riluzole for the treatment of amyotrophic lateral sclerosis, but advances in drug development and screening are substantially increasing the number of potential therapeutic agents. This review provides an overview of clinical trial methodology in amyotrophic lateral sclerosis followed by a systematic evaluation of drugs that are presently in Phase I, II and III clinical trials. There is an emphasis on the scientific evidence supporting the selection of each drug being tested, as well as on trial design
PMID: 17685869
ISSN: 1744-7658
CID: 78406