Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy
•Respiratory impairment is present in up to one-third-of patients with dysferlinopathy.•Spirometry is the gold standard for diagnosis and monitoring of respiratory impairment but is not always easily accessible.•The performance of upper limb (PUL) module is a clinical scale developed for patients wi...
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creator | Borland, Holly Moore, Ursula Dressman, Heather Gordish Human, Anri Mayhew, Anna G. Hilsden, Heather Rufibach, Laura E. Duong, Tina Maron, Elke DeWolf, Brittney Rose, Kristy Siener, Catherine Thiele, Simone Práxedes, Nieves Sanchez-Aguilera Canal, Aurélie Holsten, Scott Sakamoto, Chikako Pedrosa-Hernández, Irene Bello, Luca Alfano, Lindsay N Lowes, Linda Pax James, Meredith K. Straub, Volker |
description | •Respiratory impairment is present in up to one-third-of patients with dysferlinopathy.•Spirometry is the gold standard for diagnosis and monitoring of respiratory impairment but is not always easily accessible.•The performance of upper limb (PUL) module is a clinical scale developed for patients with NMD to test upper extremity function.•There is a significant relationship between the PUL entry item and FVC in male and female patients with dysferlinopathy.•Where spirometry equipment is not available, the PUL entry item can be used to identify patients with dysferlinopathy in whom comprehensive respiratory testing is warranted.
Dysferlin-deficient limb girdle muscular dystrophy (LGMD R2), also referred to as dysferlinopathy, can be associated with respiratory muscle weakness as the disease progresses. Clinical practice guidelines recommend biennial lung function assessments in patients with dysferlinopathy to screen for respiratory impairment. However, lack of universal access to spirometry equipment and trained specialists makes regular monitoring challenging. This study investigated the use of the Performance of Upper Limb (PUL) clinical scale entry item as a low-cost screening tool to identify patients with dysferlinopathy at risk of respiratory impairment. Using data from 193 patients from the Jain Foundation's International Clinical Outcomes Study, modelling identified a significant positive relationship between the PUL entry item and forced vital capacity (FVC). Eighty-eight percent of patients with the lowest PUL entry item score of 1 presented with FVC % predicted values of |
doi_str_mv | 10.1016/j.nmd.2024.08.003 |
format | Article |
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Dysferlin-deficient limb girdle muscular dystrophy (LGMD R2), also referred to as dysferlinopathy, can be associated with respiratory muscle weakness as the disease progresses. Clinical practice guidelines recommend biennial lung function assessments in patients with dysferlinopathy to screen for respiratory impairment. However, lack of universal access to spirometry equipment and trained specialists makes regular monitoring challenging. This study investigated the use of the Performance of Upper Limb (PUL) clinical scale entry item as a low-cost screening tool to identify patients with dysferlinopathy at risk of respiratory impairment. Using data from 193 patients from the Jain Foundation's International Clinical Outcomes Study, modelling identified a significant positive relationship between the PUL entry item and forced vital capacity (FVC). Eighty-eight percent of patients with the lowest PUL entry item score of 1 presented with FVC % predicted values of <60 %, suggestive of respiratory impairment. By contrast, only 10 % of the remainder of the cohort (PUL entry item of 2 or more) had an FVC of <60 %. This relationship also held true when accounting for ambulatory status, age, and sex as possible confounding factors. In summary, our results suggest that the PUL entry item could be implemented in clinical practice to screen for respiratory impairment where spirometry is not readily available.</description><identifier>ISSN: 0960-8966</identifier><identifier>ISSN: 1873-2364</identifier><identifier>EISSN: 1873-2364</identifier><identifier>DOI: 10.1016/j.nmd.2024.08.003</identifier><identifier>PMID: 39178649</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Adolescent ; Adult ; Aged ; Dysferlin ; Dysferlin - genetics ; Female ; Forced vital capacity ; Humans ; Limb girdle muscular dystrophy ; Male ; Middle Aged ; Miyoshi myopathy ; Muscular Dystrophies, Limb-Girdle - diagnosis ; Muscular Dystrophies, Limb-Girdle - genetics ; Muscular Dystrophies, Limb-Girdle - physiopathology ; Performance of upper limb (PUL) ; Respiratory function ; Respiratory Function Tests ; Spirometry ; Upper Extremity - physiopathology ; Vital Capacity ; Young Adult</subject><ispartof>Neuromuscular disorders : NMD, 2024-10, Vol.43, p.20-28</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c235t-4749372ec7ca02079a6c051cd49fef4f0b0f8fc57e0644a062f4ca912ef40af23</cites><orcidid>0000-0001-9046-3540</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0960896624009131$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39178649$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Borland, Holly</creatorcontrib><creatorcontrib>Moore, Ursula</creatorcontrib><creatorcontrib>Dressman, Heather Gordish</creatorcontrib><creatorcontrib>Human, Anri</creatorcontrib><creatorcontrib>Mayhew, Anna G.</creatorcontrib><creatorcontrib>Hilsden, Heather</creatorcontrib><creatorcontrib>Rufibach, Laura E.</creatorcontrib><creatorcontrib>Duong, Tina</creatorcontrib><creatorcontrib>Maron, Elke</creatorcontrib><creatorcontrib>DeWolf, Brittney</creatorcontrib><creatorcontrib>Rose, Kristy</creatorcontrib><creatorcontrib>Siener, Catherine</creatorcontrib><creatorcontrib>Thiele, Simone</creatorcontrib><creatorcontrib>Práxedes, Nieves Sanchez-Aguilera</creatorcontrib><creatorcontrib>Canal, Aurélie</creatorcontrib><creatorcontrib>Holsten, Scott</creatorcontrib><creatorcontrib>Sakamoto, Chikako</creatorcontrib><creatorcontrib>Pedrosa-Hernández, Irene</creatorcontrib><creatorcontrib>Bello, Luca</creatorcontrib><creatorcontrib>Alfano, Lindsay N</creatorcontrib><creatorcontrib>Lowes, Linda Pax</creatorcontrib><creatorcontrib>James, Meredith K.</creatorcontrib><creatorcontrib>Straub, Volker</creatorcontrib><title>Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy</title><title>Neuromuscular disorders : NMD</title><addtitle>Neuromuscul Disord</addtitle><description>•Respiratory impairment is present in up to one-third-of patients with dysferlinopathy.•Spirometry is the gold standard for diagnosis and monitoring of respiratory impairment but is not always easily accessible.•The performance of upper limb (PUL) module is a clinical scale developed for patients with NMD to test upper extremity function.•There is a significant relationship between the PUL entry item and FVC in male and female patients with dysferlinopathy.•Where spirometry equipment is not available, the PUL entry item can be used to identify patients with dysferlinopathy in whom comprehensive respiratory testing is warranted.
Dysferlin-deficient limb girdle muscular dystrophy (LGMD R2), also referred to as dysferlinopathy, can be associated with respiratory muscle weakness as the disease progresses. Clinical practice guidelines recommend biennial lung function assessments in patients with dysferlinopathy to screen for respiratory impairment. However, lack of universal access to spirometry equipment and trained specialists makes regular monitoring challenging. This study investigated the use of the Performance of Upper Limb (PUL) clinical scale entry item as a low-cost screening tool to identify patients with dysferlinopathy at risk of respiratory impairment. Using data from 193 patients from the Jain Foundation's International Clinical Outcomes Study, modelling identified a significant positive relationship between the PUL entry item and forced vital capacity (FVC). Eighty-eight percent of patients with the lowest PUL entry item score of 1 presented with FVC % predicted values of <60 %, suggestive of respiratory impairment. By contrast, only 10 % of the remainder of the cohort (PUL entry item of 2 or more) had an FVC of <60 %. This relationship also held true when accounting for ambulatory status, age, and sex as possible confounding factors. In summary, our results suggest that the PUL entry item could be implemented in clinical practice to screen for respiratory impairment where spirometry is not readily available.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Dysferlin</subject><subject>Dysferlin - genetics</subject><subject>Female</subject><subject>Forced vital capacity</subject><subject>Humans</subject><subject>Limb girdle muscular dystrophy</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Miyoshi myopathy</subject><subject>Muscular Dystrophies, Limb-Girdle - diagnosis</subject><subject>Muscular Dystrophies, Limb-Girdle - genetics</subject><subject>Muscular Dystrophies, Limb-Girdle - physiopathology</subject><subject>Performance of upper limb (PUL)</subject><subject>Respiratory function</subject><subject>Respiratory Function Tests</subject><subject>Spirometry</subject><subject>Upper Extremity - physiopathology</subject><subject>Vital Capacity</subject><subject>Young Adult</subject><issn>0960-8966</issn><issn>1873-2364</issn><issn>1873-2364</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1vFDEQhi0URC6BH0CDXKbZzdjrs9eiQhGQSJFCAbXls8fg035heyOd-PP4dEnKTDPFPO8rzUPIRwYtAyav9-00-pYDFy30LUD3hmxYr7qGd1KckQ1oCU2vpTwnFznvAdhWSfWOnHeaqV4KvSH_fmAKcxrt5JDOga7LgokOcdxRnEo60FhwpGWmS0IfXaEVdujpYyx2oM4u1sVSqYn6Qw6Yhjg1HkN0scZPPb9j8gPScc1uHWw6giXNy5_De_I22CHjh6d9SX59-_rz5ra5f_h-d_PlvnG825ZGKKE7xdEpZ4GD0lY62DLnhQ4YRIAdhD64rUKQQliQPAhnNeP1CDbw7pJcnXqXNP9dMRczxuxwGOyE85pNVz3VYUxXlJ1Ql-acEwazpDjadDAMzNG52Zvq3BydG-hNdV4zn57q192I_iXxLLkCn08A1icfIyaTj3qqxpjQFePn-Er9f0IflJU</recordid><startdate>202410</startdate><enddate>202410</enddate><creator>Borland, Holly</creator><creator>Moore, Ursula</creator><creator>Dressman, Heather Gordish</creator><creator>Human, Anri</creator><creator>Mayhew, Anna G.</creator><creator>Hilsden, Heather</creator><creator>Rufibach, Laura E.</creator><creator>Duong, Tina</creator><creator>Maron, Elke</creator><creator>DeWolf, Brittney</creator><creator>Rose, Kristy</creator><creator>Siener, Catherine</creator><creator>Thiele, Simone</creator><creator>Práxedes, Nieves Sanchez-Aguilera</creator><creator>Canal, Aurélie</creator><creator>Holsten, Scott</creator><creator>Sakamoto, Chikako</creator><creator>Pedrosa-Hernández, Irene</creator><creator>Bello, Luca</creator><creator>Alfano, Lindsay N</creator><creator>Lowes, Linda Pax</creator><creator>James, Meredith K.</creator><creator>Straub, Volker</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9046-3540</orcidid></search><sort><creationdate>202410</creationdate><title>Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy</title><author>Borland, Holly ; Moore, Ursula ; Dressman, Heather Gordish ; Human, Anri ; Mayhew, Anna G. ; Hilsden, Heather ; Rufibach, Laura E. ; Duong, Tina ; Maron, Elke ; DeWolf, Brittney ; Rose, Kristy ; Siener, Catherine ; Thiele, Simone ; Práxedes, Nieves Sanchez-Aguilera ; Canal, Aurélie ; Holsten, Scott ; Sakamoto, Chikako ; Pedrosa-Hernández, Irene ; Bello, Luca ; Alfano, Lindsay N ; Lowes, Linda Pax ; James, Meredith K. ; Straub, Volker</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c235t-4749372ec7ca02079a6c051cd49fef4f0b0f8fc57e0644a062f4ca912ef40af23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Dysferlin</topic><topic>Dysferlin - genetics</topic><topic>Female</topic><topic>Forced vital capacity</topic><topic>Humans</topic><topic>Limb girdle muscular dystrophy</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Miyoshi myopathy</topic><topic>Muscular Dystrophies, Limb-Girdle - diagnosis</topic><topic>Muscular Dystrophies, Limb-Girdle - genetics</topic><topic>Muscular Dystrophies, Limb-Girdle - physiopathology</topic><topic>Performance of upper limb (PUL)</topic><topic>Respiratory function</topic><topic>Respiratory Function Tests</topic><topic>Spirometry</topic><topic>Upper Extremity - physiopathology</topic><topic>Vital Capacity</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Borland, Holly</creatorcontrib><creatorcontrib>Moore, Ursula</creatorcontrib><creatorcontrib>Dressman, Heather Gordish</creatorcontrib><creatorcontrib>Human, Anri</creatorcontrib><creatorcontrib>Mayhew, Anna G.</creatorcontrib><creatorcontrib>Hilsden, Heather</creatorcontrib><creatorcontrib>Rufibach, Laura E.</creatorcontrib><creatorcontrib>Duong, Tina</creatorcontrib><creatorcontrib>Maron, Elke</creatorcontrib><creatorcontrib>DeWolf, Brittney</creatorcontrib><creatorcontrib>Rose, Kristy</creatorcontrib><creatorcontrib>Siener, Catherine</creatorcontrib><creatorcontrib>Thiele, Simone</creatorcontrib><creatorcontrib>Práxedes, Nieves Sanchez-Aguilera</creatorcontrib><creatorcontrib>Canal, Aurélie</creatorcontrib><creatorcontrib>Holsten, Scott</creatorcontrib><creatorcontrib>Sakamoto, Chikako</creatorcontrib><creatorcontrib>Pedrosa-Hernández, Irene</creatorcontrib><creatorcontrib>Bello, Luca</creatorcontrib><creatorcontrib>Alfano, Lindsay N</creatorcontrib><creatorcontrib>Lowes, Linda Pax</creatorcontrib><creatorcontrib>James, Meredith K.</creatorcontrib><creatorcontrib>Straub, Volker</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Neuromuscular disorders : NMD</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borland, Holly</au><au>Moore, Ursula</au><au>Dressman, Heather Gordish</au><au>Human, Anri</au><au>Mayhew, Anna G.</au><au>Hilsden, Heather</au><au>Rufibach, Laura E.</au><au>Duong, Tina</au><au>Maron, Elke</au><au>DeWolf, Brittney</au><au>Rose, Kristy</au><au>Siener, Catherine</au><au>Thiele, Simone</au><au>Práxedes, Nieves Sanchez-Aguilera</au><au>Canal, Aurélie</au><au>Holsten, Scott</au><au>Sakamoto, Chikako</au><au>Pedrosa-Hernández, Irene</au><au>Bello, Luca</au><au>Alfano, Lindsay N</au><au>Lowes, Linda Pax</au><au>James, Meredith K.</au><au>Straub, Volker</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy</atitle><jtitle>Neuromuscular disorders : NMD</jtitle><addtitle>Neuromuscul Disord</addtitle><date>2024-10</date><risdate>2024</risdate><volume>43</volume><spage>20</spage><epage>28</epage><pages>20-28</pages><issn>0960-8966</issn><issn>1873-2364</issn><eissn>1873-2364</eissn><abstract>•Respiratory impairment is present in up to one-third-of patients with dysferlinopathy.•Spirometry is the gold standard for diagnosis and monitoring of respiratory impairment but is not always easily accessible.•The performance of upper limb (PUL) module is a clinical scale developed for patients with NMD to test upper extremity function.•There is a significant relationship between the PUL entry item and FVC in male and female patients with dysferlinopathy.•Where spirometry equipment is not available, the PUL entry item can be used to identify patients with dysferlinopathy in whom comprehensive respiratory testing is warranted.
Dysferlin-deficient limb girdle muscular dystrophy (LGMD R2), also referred to as dysferlinopathy, can be associated with respiratory muscle weakness as the disease progresses. Clinical practice guidelines recommend biennial lung function assessments in patients with dysferlinopathy to screen for respiratory impairment. However, lack of universal access to spirometry equipment and trained specialists makes regular monitoring challenging. This study investigated the use of the Performance of Upper Limb (PUL) clinical scale entry item as a low-cost screening tool to identify patients with dysferlinopathy at risk of respiratory impairment. Using data from 193 patients from the Jain Foundation's International Clinical Outcomes Study, modelling identified a significant positive relationship between the PUL entry item and forced vital capacity (FVC). Eighty-eight percent of patients with the lowest PUL entry item score of 1 presented with FVC % predicted values of <60 %, suggestive of respiratory impairment. By contrast, only 10 % of the remainder of the cohort (PUL entry item of 2 or more) had an FVC of <60 %. This relationship also held true when accounting for ambulatory status, age, and sex as possible confounding factors. In summary, our results suggest that the PUL entry item could be implemented in clinical practice to screen for respiratory impairment where spirometry is not readily available.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>39178649</pmid><doi>10.1016/j.nmd.2024.08.003</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-9046-3540</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Dysferlin Dysferlin - genetics Female Forced vital capacity Humans Limb girdle muscular dystrophy Male Middle Aged Miyoshi myopathy Muscular Dystrophies, Limb-Girdle - diagnosis Muscular Dystrophies, Limb-Girdle - genetics Muscular Dystrophies, Limb-Girdle - physiopathology Performance of upper limb (PUL) Respiratory function Respiratory Function Tests Spirometry Upper Extremity - physiopathology Vital Capacity Young Adult |
title | Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy |
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