 | Samantha LevineGreat Ormond Street Hospital for Children, London, United Kingdom | Department of Cellular Pathology, St George’s Healthcare Trust, London, UK | Department of Psychology, ... |
Is this your profile? Claim your profile Copy URL Embed Link to your profile |
Samantha Levine:Expert Impact
Concepts for whichSamantha Levinehas direct influence:Hereditary leiomyomatosis,Behavior therapy,Renal cancer,Patients stridor,Therapeutic alliance,Patients msa,Multiple atrophy msa,Renal cell carcinoma.
Samantha Levine:KOL impact
Concepts related to the work of other authors for whichfor which Samantha Levine has influence:Multiple atrophy,Hereditary leiomyomatosis,Movement disorders,Patients msa,Renal cell carcinoma,Sleep apnea,Autonomic failure.
KOL Resume for Samantha Levine
| Year | |
|---|---|
| 2020 | Great Ormond Street Hospital for Children, London, United Kingdom |
| 2009 | Department of Cellular Pathology, St George’s Healthcare Trust, London, UK |
| 2005 | Department of Psychology, University of Marland |
| 2000 | Mayo Sleep Disorders Center, Mayo Clinic, Rochester, Minnesota, U.S.A. |
| Concept | World rank |
|---|---|
| msa death | #9 |
| death multiple atrophy | #14 |
| msa stridor | #27 |
| msa survival | #33 |
| patients stridor | #43 |
| nocturnal stridor | #84 |
Prominent publications by Samantha Levine
Patients with multiple system atrophy (MSA) have a mean survival of 8 to 10 years. Nocturnal stridor has been considered a poor prognostic feature. We analyzed demographic, clinical, and polysomnographic data and obtained follow-up information from 42 patients with MSA (30 with follow-up data) seen in a Sleep Disorders Center. Group I consisted of 17 patients with nocturnal stridor, including seven with daytime stridor. Group II consisted of 25 patients without stridor. Analysis of ...
| Known for Patients Stridor | Multiple Atrophy Msa | Central Hypoventilation | Shorter Survival | Disease Onset |
Hereditary leiomyomatosis and renal cell carcinoma: very early diagnosis of renal cancer in a paediatric patient
[ PUBLICATION ]
Hereditary leiomyomatosis and renal cell cancer is a hereditary cancer syndrome in which affected individuals are at risk for cutaneous and uterine leiomyomas, and renal cancer. Previous reports have stressed the aggressiveness of the renal tumours, often with early metastasis, despite small primary tumour size. Almost all the previously reported patients were adults, and different studies showed variability in penetrance for the renal tumours. We report a patient in whom renal cancer ...
| Known for Hereditary Leiomyomatosis | Renal Cancer | Cell Carcinoma | 11 Years | Cutaneous Uterine Leiomyomas |
It may be argued that behavior therapy has proceeded with minimal regard for the therapeutic alliance (TA) as a key mechanism of change. However, ignoring the role of TA in behavior therapy may not only be problematic on a practical level, but also may be inconsistent with basic principles that underlie behavior therapy. In beginning to address these issues, the authors consider the role of TA in behavior therapy with a focus on relevant basic principles. Keeping a focus on these basic ...
| Known for Behavior Therapy | Therapeutic Alliance |
Colonic Basidiobolomycosis—An Unusual Presentation of Eosinophilic Intestinal Inflammation
[ PUBLICATION ]
Basidiobolomycosis is a rare fungal disease caused by Basidiobolus ranarum. Involvement of the gastrointestinal tract is unusual and poses both a diagnostic and therapeutic challenge, as clinical signs are non-specific and predisposing risk factors are lacking. It can mimick inflammatory bowel disease, primary immunodeficiency, or a malignancy and should be considered in patients who do not respond to standard therapy. We present the case of a 22 months old boy with confirmed colonic ...
| Known for Gastrointestinal Tract |
