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25 citation(s) found for "Watson, James".

Occipital neuralgia associates with high cervical spinal cord lesions in idiopathic inflammatory demyelinating disease
Kissoon, Narayan , Watson, James C. , Kantarci, Orhun H. , Kissoon, Narayan R , Boes, Christopher J.

Mayo Clinic

Cephalalgia | April 9, 2018 | Volume: 39 | Issue: 1 | Pages: 21-28

10.1177/0333102418769953 | PMID 29629601 Get It

Background The association of trigeminal neuralgia with pontine lesions has been well documented in multiple sclerosis, and we tested the hypothesis that occipital neuralgia in multiple sclerosis is associated with high cervical spinal cord lesions. Methods We retrospectively reviewed the records of 29 patients diagnosed with both occipital neuralgia and demyelinating disease by a neurologist from January 2001 to December 2014. We collected data on demographics, clinical findings, presence of C2-3 demyelinating lesions, and treatment responses. Results The patients with both occipital neuralgia and multiple sclerosis were typically female (76%) and had a later onset (age > 40) of occipital neuralgia (72%). Eighteen patients (64%) had the presence of C2-3 lesions and the majority had unilateral symptoms (83%) or episodic pain (78%). All patients with documented sensory loss (3/3) had C2-3 lesions. Most patients with progressive multiple sclerosis (6/8) had C2-3 lesions. Of the eight patients with C2-3 lesions and imaging at onset of occipital neuralgia, five (62.5%) had evidence of active demyelination. None of the patients with progressive multiple sclerosis (3/3) responded to occipital nerve blocks or high dose intravenous steroids, whereas all of the other phenotypes with long term follow-up (eight patients) had good responses. Conclusions A cervical spine MRI should be considered in all patients presenting with occipital neuralgia. In patients with multiple sclerosis, clinical features in occipital neuralgia that were predictive of the presence of a C2-3 lesion were unilateral episodic symptoms, sensory loss, later onset of occipital neuralgia, and progressive multiple sclerosis phenotype. Clinical phenotype predicted response to treatment.
Deep Venous Thrombosis and Bilateral Pulmonary Embolism Revealing Silent Celiac Disease: Case Report and Review of the Literature
Dumic, Igor , Martin, Scott, Salfiti, Nadim, Alempijević, Tamara , Watson, Robert, Alempijevic, Tamara , Dumic, Igor , Watson, Robert James

Mayo Clinic

Case Reports in Gastrointestinal Medicine | December 12, 2017 | Volume: 2017 | Issue: No issue available | Pages: 1-8

10.1155/2017/5236918 | PMID 29379656 Get It

Celiac disease (CD) is a systemic, chronic autoimmune disease that occurs in genetically predisposed individuals following dietary gluten exposure. CD can present with a wide range of gastrointestinal and extraintestinal manifestations and requires lifelong adherence to a gluten-free diet [GFD]. Venous thromboembolism (VTE) as a presentation of celiac disease is unusual and rarely reported. We present a case of a 46-year-old man who was admitted for shortness of breath and pleuritic chest pain and was found to have iron deficiency anemia, deep venous thrombosis, and bilateral pulmonary emboli (PE). After work-up for his anemia, the patient was diagnosed with CD. Comprehensive investigation for inherited or acquired prothrombotic disorders was negative. It is becoming increasingly recognized that CD is associated with an increased risk for VTE. PE, however, as a presentation of CD is exceedingly rare and to the best of our knowledge this is the third case report of such an occurrence and the only case report of a patient from North America. It is important to recognize that the first symptoms or signs of celiac disease might be extraintestinal. Furthermore, VTE as a presentation of CD is rare but life-threatening.
Association of Long-term Opioid Therapy With Functional Status, Adverse Outcomes, and Mortality Among Patients With Polyneuropathy
Hoffman, E. Matthew , Watson, James C. , Sauver, Jennifer L. St. , Staff, Nathan P. , Klein, Christopher J. , St Sauver, Jennifer, Staff, Nathan P , Klein, Christopher J , St Sauver, Jennifer L

Mayo Clinic

JAMA Neurology | May 22, 2017 | Volume: 74 | Issue: 7 | Pages: 773

10.1001/jamaneurol.2017.0486 | PMID 28531306 Get It

Validity and feasibility of the EMG direct observation tool (EMG-DOT)
Rubin, Devon I., Laughlin, Ruple S. , Sorenson, Eric J. , Watson, James C. , Jones, Lyell K. , Juul, Dorthea, Park, Yoon Soo , Leep Hunderfund, Andrea N, Hunderfund, Andrea N. Leep , Park, Yoon Soo , Jones, Lyell K

Mayo Clinic

Neurology | March 31, 2016 | Volume: 86 | Issue: 17 | Pages: 1627-1634

10.1212/wnl.0000000000002609 | PMID 27029634 Get It

Poster 532 Sacral Tumors Confounding the Diagnosis of Muscular Dystrophy: A Case Report
Brubaker, Morgan, Presley, Jim, Watson, James B.

Mayo Clinic

PM&R | September 29, 2014 | Volume: 6 | Issue: 9S | Pages: No page available

10.1016/j.pmrj.2014.08.898 Get It

Sensitivity and specificity of diagnostic ultrasound in the diagnosis of phrenic neuropathy
Boon, Andrea J. , Sekiguchi, Hiroshi , Harper, Caitlin J., Strommen, Jeffrey A., Ghahfarokhi, Leili Shahgholi, Watson, James C. , Sorenson, Eric J. , Ghahfarokhi, Leili S

Mayo Clinic

Neurology | August 28, 2014 | Volume: 83 | Issue: 14 | Pages: 1264-1270

10.1212/wnl.0000000000000841 | PMID 25165390 Get It

From the notch to a glioma grading system: the neurological contributions of James Watson Kernohan
Safavi‐Abbasi, Sam, Maurer, Adrian J., Archer, Jacob, Sughrue, Michael E. , Hanel, Ricardó A. , Theodore, Nicholas , Preul, Mark C.

Mayo Clinic

Neurosurgical Focus | April 1, 2014 | Volume: 36 | Issue: 4 | Pages: E4

10.3171/2014.1.focus13575 | PMID 24684337 Get It

During his lifetime and a career spanning 42 years, James Watson Kernohan made numerous contributions to neuropathology, neurology, and neurosurgery. One of these, the phenomenon of ipsilateral, false localizing signs caused by compression of the contralateral cerebral peduncle against the tentorial edge, has widely become known as “Kernohan's notch” and continues to bear his name. The other is a grading system for gliomas from a neurosurgical viewpoint that continues to be relevant for grading of glial tumors 60 years after its introduction. In this paper, the authors analyze these two major contributions in detail within the context of Kernohan's career and explore how they contributed to the development of neurosurgical procedures.
Clinical, electrophysiologic, and imaging features of zoster‐associated limb paresis
Jones, Lyell K. , Haatem, Reda, Watson, James C. , Jones, Lyell K

Mayo Clinic

Muscle & Nerve | December 4, 2013 | Volume: 50 | Issue: 2 | Pages: 177-185

10.1002/mus.24141 | PMID 24638224 Get It

ABSTRACTIntroduction: Paresis is a long‐recognized complication of herpes zoster, but there has been comparatively little study of zoster‐associated limb paresis (ZALP). Methods: In this study we reviewed 49 Mayo Clinic patients with ZALP. Results: The mean age of onset was 71 years, 67% were men, and the lower limb was affected in 55%. The mean weakness score was 2.0 (0 = normal strength, 4 = plegia). Most patients developed postherpetic neuralgia (PHN, 92% at 1 month and 65% at 3 months), and the average minimum duration of weakness was 193 days. ZALP was caused by radiculopathy (37%), plexopathy (41%), mononeuropathy (14%), and radiculoplexus neuropathy (8%). MRI demonstrated nerve enlargement, T2 signal prolongation, or enhancement in a majority (64%) of affected plexi and peripheral nerves. Conclusions: ZALP is associated with considerable weakness. It typically lasts at least several months, localizes to plexus or peripheral nerve in 63%, and is associated with high rates of PHN. Muscle Nerve 50:177–185, 2014
Diaphragm depth in normal subjects
Shahgholi, Leili , Baria, Michael R. , Sorenson, Eric J. , Harper, Caitlin J., Watson, James C. , Strommen, Jeffrey A., Boon, Andrea J.

Mayo Clinic

Muscle & Nerve | July 19, 2013 | Volume: 49 | Issue: 5 | Pages: 666-668

10.1002/mus.23953 | PMID 23873396 Get It

ABSTRACTIntroduction: Needle electromyography (EMG) of the diaphragm carries the potential risk of pneumothorax. Knowing the approximate depth of the diaphragm should increase the test's safety and accuracy. Methods: Distances from the skin to the diaphragm and from the outer surface of the rib to the diaphragm were measured using B mode ultrasound in 150 normal subjects. Results: When measured at the lower intercostal spaces, diaphragm depth varied between 0.78 and 4.91 cm beneath the skin surface and between 0.25 and 1.48 cm below the outer surface of the rib. Using linear regression modeling, body mass index (BMI) could be used to predict diaphragm depth from the skin to within an average of 1.15 mm. Conclusions: Diaphragm depth from the skin can vary by more than 4 cm. When image guidance is not available to enhance accuracy and safety of diaphragm EMG, it is possible to reliably predict the depth of the diaphragm based on BMI. Muscle Nerve 49: 666–668, 2014
Two‐dimensional ultrasound imaging of the diaphragm: Quantitative values in normal subjects
Boon, Andrea J. , Harper, Caitlin J., Ghahfarokhi, Leili Shahgholi, Strommen, Jeffrey A., Watson, James C. , Sorenson, Eric J.

Mayo Clinic

Muscle & Nerve | October 16, 2012 | Volume: 47 | Issue: 6 | Pages: 884-889

10.1002/mus.23702 | PMID 23625789 Get It

Introduction : Real time ultrasound imaging of the diaphragm is an under‐used tool in the evaluation of patients with unexplained dyspnea or respiratory failure. Methods : We measured diaphragm thickness and the change in thickness that occurs with maximal inspiration in 150 normal subjects, with results stratified for age, gender, body mass index, and smoking history. Results : The lower limit of normal diaphragm thickness at end expiration or functional residual capacity is 0.15 cm, and an increase of at least 20% in diaphragm thickness from functional residual capacity to total lung capacity is normal. A side to side difference in thickness at end expiration of > 0.33 cm is abnormal. Diaphragm thickness and contractility are minimally affected by age, gender, body habitus, or smoking history. Conclusions : This study confirms previous findings in much smaller groups of normal controls for quantitative ultrasound of the diaphragm and provides data that can be applied widely to the general population. Muscle Nerve 47: 884–889, 2013