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  1. Article: Le jubilé de diamant de

    Harris, Susan R

    Physiotherapy Canada. Physiotherapie Canada

    2023  Volume 75, Issue 2, Page(s) 101–104

    Language English
    Publishing date 2023-05-01
    Publishing country Canada
    Document type Editorial
    ZDB-ID 639189-8
    ISSN 1708-8313 ; 0300-0508
    ISSN (online) 1708-8313
    ISSN 0300-0508
    DOI 10.3138/ptc-2023-01-31-fr
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Physiotherapy Canada's

    Harris, Susan R

    Physiotherapy Canada. Physiotherapie Canada

    2023  Volume 75, Issue 2, Page(s) 97–100

    Language English
    Publishing date 2023-05-01
    Publishing country Canada
    Document type Editorial
    ZDB-ID 639189-8
    ISSN 1708-8313 ; 0300-0508
    ISSN (online) 1708-8313
    ISSN 0300-0508
    DOI 10.3138/ptc-2023-01-31-gee
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: A rare but persistent cause of decreased function secondary to adjuvant radiation therapy in women with breast cancer.

    Harris, Susan R

    Breast cancer research and treatment

    2023  Volume 198, Issue 1, Page(s) 185–186

    MeSH term(s) Female ; Humans ; Breast Neoplasms/drug therapy ; Radiotherapy, Adjuvant/adverse effects ; Combined Modality Therapy ; Mastectomy, Segmental ; Chemotherapy, Adjuvant
    Language English
    Publishing date 2023-01-05
    Publishing country Netherlands
    Document type Letter ; Comment
    ZDB-ID 604563-7
    ISSN 1573-7217 ; 0167-6806
    ISSN (online) 1573-7217
    ISSN 0167-6806
    DOI 10.1007/s10549-022-06854-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Growing up with Marshall syndrome: A case report from infancy to age 12.5 years.

    Harris, Susan R

    American journal of medical genetics. Part A

    2023  Volume 194, Issue 4, Page(s) e63488

    Abstract: Marshall syndrome is an extremely rare genetic disorder usually diagnosed in infancy with a prevalence of <1 in 1 million. Based on the literature reviewed, this is the first case report to provide a longitudinal history of a child with Marshall syndrome ...

    Abstract Marshall syndrome is an extremely rare genetic disorder usually diagnosed in infancy with a prevalence of <1 in 1 million. Based on the literature reviewed, this is the first case report to provide a longitudinal history of a child with Marshall syndrome (from birth to age 12.5 years). This longitudinal case report arose in part from desires of this child's parents to share the story of their early fears at her initial diagnosis and compare those to how well she has turned out.
    MeSH term(s) Humans ; Child ; Female ; Mutation ; Osteochondrodysplasias/diagnosis ; Osteochondrodysplasias/genetics ; Craniofacial Abnormalities/genetics ; Hearing Loss, Sensorineural/genetics ; Syndrome ; Cataract ; Collagen Type XI/deficiency
    Chemical Substances Collagen Type XI
    Language English
    Publishing date 2023-12-07
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2108614-X
    ISSN 1552-4833 ; 0148-7299 ; 1552-4825
    ISSN (online) 1552-4833
    ISSN 0148-7299 ; 1552-4825
    DOI 10.1002/ajmg.a.63488
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Brachial plexopathy after breast cancer: A persistent late effect of radiotherapy.

    Harris, Susan R

    PM & R : the journal of injury, function, and rehabilitation

    2023  Volume 16, Issue 1, Page(s) 85–91

    Abstract: Radiation-induced brachial plexopathy (RIBP) is an iatrogenic, progressively disabling, and often very late effect of adjuvant radiotherapy most commonly seen in breast cancer survivors but also in those treated for lymphoma, lung, and head and neck ... ...

    Abstract Radiation-induced brachial plexopathy (RIBP) is an iatrogenic, progressively disabling, and often very late effect of adjuvant radiotherapy most commonly seen in breast cancer survivors but also in those treated for lymphoma, lung, and head and neck cancers. In late-onset RIBP following breast cancer, the nerve injury is chronic and irreversible, occurring more commonly when axillary and/or supraclavicular nodes have been irradiated, as well as the breast/chest wall. RIBP is manifested initially by paresthesia, hypoesthesia, dysesthesia, and later by weakness in the ipsilateral hand with those symptoms progressing distally to proximally up through the shoulder. Depressed/absent deep tendon reflexes in the upper extremity and muscle fasciculations occur also. Neither patients nor their health care providers tend to associate these unusual neurological symptoms with cancer treatments received ≥20 years prior, often failing to link these sensory-motor symptoms with radiotherapy decades before. Because long-term follow-up of these patients now typically falls to general practitioners, many cases may be missed or misdiagnosed because of the rarity of this disorder. Physiatrists and allied rehabilitation professionals must be aware of this progressively disabling, incurable condition to provide appropriate diagnoses and compensatory rehabilitation therapies. Additionally, professional oncology organizations should include RIBP in their long-term, survivorship guidelines for breast cancer. Researchers examining the iatrogenic late effects of radiotherapy should extend their follow-up periods well beyond the current 5-6 years to ascertain the true incidence of RIBP today. Rehabilitation providers must continue to advocate for awareness, diagnosis, and management of iatrogenic outcomes experienced by long-term cancer survivors.
    MeSH term(s) Humans ; Female ; Breast Neoplasms/radiotherapy ; Breast Neoplasms/complications ; Brachial Plexus Neuropathies/diagnosis ; Brachial Plexus Neuropathies/etiology ; Neck ; Iatrogenic Disease ; Radiation Injuries
    Language English
    Publishing date 2023-07-31
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2608988-9
    ISSN 1934-1563 ; 1934-1482
    ISSN (online) 1934-1563
    ISSN 1934-1482
    DOI 10.1002/pmrj.13007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Revisiting the Case for Case Reports.

    Harris, Susan R

    Physical therapy

    2019  Volume 99, Issue 9, Page(s) 1122–1125

    MeSH term(s) Evidence-Based Medicine ; Exercise ; Female ; Humans ; Lymphedema/etiology ; Lymphedema/pathology ; Medical Records/statistics & numerical data ; Physical Therapy Specialty/statistics & numerical data ; Physical Therapy Specialty/trends ; Publishing/statistics & numerical data ; Publishing/trends ; Randomized Controlled Trials as Topic ; Systematic Reviews as Topic ; Upper Extremity
    Language English
    Publishing date 2019-06-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 415886-6
    ISSN 1538-6724 ; 0031-9023
    ISSN (online) 1538-6724
    ISSN 0031-9023
    DOI 10.1093/ptj/pzz081
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Ovarian cancer metastases to internal mammary nodes.

    Harris, Susan R

    The breast journal

    2019  Volume 25, Issue 2, Page(s) 351–352

    MeSH term(s) Adult ; Aged ; BRCA2 Protein/genetics ; Breast Neoplasms/genetics ; Breast Neoplasms/secondary ; Female ; Humans ; Hysterectomy ; Lymph Nodes/pathology ; Lymphatic Metastasis/pathology ; Middle Aged ; Ovarian Neoplasms/drug therapy ; Ovarian Neoplasms/pathology ; Ovarian Neoplasms/surgery
    Chemical Substances BRCA2 Protein ; BRCA2 protein, human
    Language English
    Publishing date 2019-02-06
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 1289960-4
    ISSN 1524-4741 ; 1075-122X
    ISSN (online) 1524-4741
    ISSN 1075-122X
    DOI 10.1111/tbj.13226
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Psychogenic movement disorders in children and adolescents: an update.

    Harris, Susan R

    European journal of pediatrics

    2019  Volume 178, Issue 4, Page(s) 581–585

    Abstract: This short communication provides an update on childhood psychogenic movement disorders (PMD), focusing on descriptive studies and case reports from 2008 to 2018. Known also as functional movement/motor disorders, PMD diagnoses are relatively common in ... ...

    Abstract This short communication provides an update on childhood psychogenic movement disorders (PMD), focusing on descriptive studies and case reports from 2008 to 2018. Known also as functional movement/motor disorders, PMD diagnoses are relatively common in adults but less so in children. In group studies over the past decade, sample prevalence of childhood PMD ranged from 2.8 to 23.1%, with a higher percentage of girls in most studies (consistent with adult PMD literature). Common types of PMD included tremor (32.4%), dystonia (29.5%), and myoclonus (24.3%). Precipitating events for PMD onset included H1N1 influenza vaccinations, family/child stressors, anxiety/depression in the child or parent, panic attacks, behavior disorders, injury or accident, sexual abuse of the child or family member, death of a close relative, parental discord, domestic violence, school-related problems, medical illness/surgery, sleep disturbance, and participation in competitive sport or dance. The most frequently mentioned treatments were cognitive behavioral therapy, psychotherapy, relaxation techniques, and physiotherapy.Conclusion: Although additional cases of childhood PMD have been published over the past decade, little new information has appeared. There is still no "diagnostic gold standard," making an accurate estimate of prevalence virtually impossible and contributing to confusion among pediatricians when trying to identify children with PMD. What is Known: • Psychogenic movement disorders (PMD) occur in children as well as adults. • The most common types of childhood PMD are tremor, dystonia, and myoclonus. What is New: • The most common childhood PMD treatments were cognitive behavioral therapy, psychotherapy, physiotherapy, and relaxation techniques (2008-2018). • Due to lack of a standardized definition for PMD, confusion exists as to which movement disorders to include. With the inability to reliably diagnose PMD and the ambiguity as to which movement disorders it comprises, it is difficult to determine the most effective treatments.
    MeSH term(s) Adolescent ; Child ; Female ; Humans ; Male ; Movement Disorders/diagnosis ; Movement Disorders/epidemiology ; Movement Disorders/therapy
    Language English
    Publishing date 2019-01-11
    Publishing country Germany
    Document type Journal Article ; Review
    ZDB-ID 194196-3
    ISSN 1432-1076 ; 0340-6199 ; 0943-9676
    ISSN (online) 1432-1076
    ISSN 0340-6199 ; 0943-9676
    DOI 10.1007/s00431-019-03317-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Teachers' Perceptions of Handwriting Legibility Versus the German Systematic Screening for Motoric-Handwriting Difficulties (SEMS).

    Franken, Anita M / Harris, Susan R

    OTJR : occupation, participation and health

    2021  Volume 41, Issue 4, Page(s) 251–258

    Abstract: Handwriting problems impact school achievement. The purpose of this pilot study was to evaluate the agreement between teachers' opinions and the German Systematische Erfassung motorischer Schreibstörungen's (SEMS) handwriting test and to estimate the ... ...

    Abstract Handwriting problems impact school achievement. The purpose of this pilot study was to evaluate the agreement between teachers' opinions and the German Systematische Erfassung motorischer Schreibstörungen's (SEMS) handwriting test and to estimate the prevalence of handwriting problems. This was a prospective, correlational study. Teachers' ratings of handwriting from German children (Grades 2 and 4) were compared to SEMS scores. The agreement was calculated with Gwet's AC2; preliminary cutoffs and prevalence were assessed with receiver-operating characteristic curves. SEMS accurately identified Grade 2 children with handwriting problems (specificity = 98.21%, sensitivity = 100%) but fewer Grade 4 children with handwriting difficulties than did teachers (specificity 97.67%, sensitivity 28.57%). Grade 4 item agreement supports the SEMS' ability to assess underlying handwriting dimensions as perceived by teachers. Teachers identified 12.70% of Grade 2 children versus SEMS 11.11% and 14% of Grade 4 children versus SEMS 6%. The SEMS supports clinical observations and provides information about underlying handwriting dimensions. Because handwriting is used primarily at school, the opinions of teachers are also critical.
    MeSH term(s) Child ; Handwriting ; Humans ; Perception ; Pilot Projects ; Prospective Studies ; Schools
    Language English
    Publishing date 2021-07-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2081243-7
    ISSN 1938-2383 ; 1539-4492 ; 0276-1599
    ISSN (online) 1938-2383
    ISSN 1539-4492 ; 0276-1599
    DOI 10.1177/15394492211033828
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Axillary Web Syndrome in Breast Cancer: A Prevalent But Under-Recognized Postoperative Complication.

    Harris, Susan R

    Breast care (Basel, Switzerland)

    2018  Volume 13, Issue 2, Page(s) 132–135

    Abstract: The purpose of this review is to define axillary web syndrome (AWS) and describe its diagnosis and management. The following databases were searched through July 2017: PubMed, EMBASE (OvidSP), Cumulative Index for Nursing and Allied Health Literature, ... ...

    Abstract The purpose of this review is to define axillary web syndrome (AWS) and describe its diagnosis and management. The following databases were searched through July 2017: PubMed, EMBASE (OvidSP), Cumulative Index for Nursing and Allied Health Literature, Physiotherapy Evidence Database, and Cochrane Database of Systematic Reviews. Search terms included 'axillary web syndrome', 'axillary cording', and 'lymphatic cording'. 49 articles were identified; 8 did not relate to breast cancer, and 3 were not in English. Of the remaining articles, the majority were case reports, case series, or descriptive reviews. 2 systematic reviews were located as well as 1 randomized trial, 6 prospective cohort studies, and 2 retrospective cohort studies. Although a common sequela after axillary surgery for breast cancer staging, AWS has been poorly described in the medical literature as to the underlying pathophysiology, diagnosis, and management. Interventions range from patient education and simple reassurance that the syndrome will resolve spontaneously to active physical or manual therapies to maintain upper extremity range-of-motion, especially adequate motion for undergoing radiation therapy. Oncologists, breast surgeons, family physicians, and oncology nurse practitioners that work with patients with breast cancer should educate them about this prevalent complication and inform them preoperatively about what to anticipate.
    Language English
    Publishing date 2018-02-01
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2202236-3
    ISSN 1661-3805 ; 1661-3791
    ISSN (online) 1661-3805
    ISSN 1661-3791
    DOI 10.1159/000485023
    Database MEDical Literature Analysis and Retrieval System OnLINE

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