{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,20]],"date-time":"2026-02-20T23:13:54Z","timestamp":1771629234280,"version":"3.50.1"},"reference-count":30,"publisher":"BMJ","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Neurology, Neurosurgery & Psychiatry"],"published-print":{"date-parts":[[1972,4,1]]},"DOI":"10.1136\/jnnp.35.2.208","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T21:02:42Z","timestamp":1226350962000},"page":"208-215","source":"Crossref","is-referenced-by-count":77,"title":["X-linked scapuloperoneal syndrome"],"prefix":"10.1136","volume":"35","author":[{"given":"P. K.","family":"Thomas","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D. B.","family":"Calne","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C. F.","family":"Elliott","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","reference":[{"key":"ref_1","first-page":"208","article-title":"Mental retardation in association with progressive muscular dystrophy","volume":"100","author":"Allen, J.E.; Rodgin, D.W.","year":"1960","unstructured":"Allen, J. E., and Rodgin, D. W. (1960). Mental retardation in association with progressive muscular dystrophy. Amnericanz Journal of Diseases of Children, 100, 208-211.","journal-title":"Amnericanz Journal of Diseases of Children"},{"issue":"303-3","key":"ref_2","first-page":"10","article-title":"Neue Ergebnisse der Genetik der Muskeldystrophien","volume":"7","author":"Becker, P.E.","year":"1957","unstructured":"Becker, P. E. (1957). Neue Ergebnisse der Genetik der Muskeldystrophien. Acta Genetica et Statistica Medica, 7, 303-3 10.","journal-title":"Acta Genetica et Statistica Medica"},{"key":"ref_3","first-page":"551","article-title":"Two new families of benign sex-linked recessive muscular dystrophy","volume":"21","author":"Becker, P.E.","year":"1962","unstructured":"Becker, P. E. (1962). Two new families of benign sex-linked recessive muscular dystrophy. Revue Canadientne de Biologie, 21, 551-566.","journal-title":"Revue Canadientne de Biologie"},{"key":"ref_4","first-page":"427","article-title":"Eine neue X-chromosomale Muskeldystrophie. Archiv fur Psychiatrie untid Nervenkrankheiten vereinigt mit Zeitschrift fiir die gesamtite Neurologie und","volume":"193","author":"Becker, P.F.; Keiner, F.","year":"1955","unstructured":"Becker, P. F., and Keiner, F. (1955). Eine neue X-chromosomale Muskeldystrophie. Archiv fur Psychiatrie untid Nervenkrankheiten vereinigt mit Zeitschrift fiir die gesamtite Neurologie und Psychiatrie, 193, 427-448.","journal-title":"Psychiatrie"},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1001\/archneurpsyc.1953.02320310007001","article-title":"Progressive neuropathic (peroneal) muscular atrophy (CharcotMarie-Tooth disease). Histological findings in muscle biopsy specimens in fourteen cases, with notes on clinical diagnosis and familial occurrence","volume":"70","author":"Brodal, A.; Boyesen, S.; Frbvig, A.G.","year":"1953","unstructured":"Brodal, A., Boyesen, S., and Frbvig, A. G. (1953). Progressive neuropathic (peroneal) muscular atrophy (CharcotMarie-Tooth disease). Histological findings in muscle biopsy specimens in fourteen cases, with notes on clinical diagnosis and familial occurrence. Archives of Neurology and Psychiatry, 70, 1-29.","journal-title":"Archives of Neurology and Psychiatry"},{"key":"ref_6","article-title":"Etude Clinique sur utne Fortmze Hereditaire d'Atrophie Musculaire Progressive Debutant par les Membres Inferieurs (Type Femnoral av ec Griffes des Orteils)","author":"Brossard, J.","year":"1886","unstructured":"Brossard, J. (1886). Etude Clinique sur utne Fortmze Hereditaire d'Atrophie Musculaire Progressive Debutant par les Membres Inferieurs (Type Femnoral av ec Griffes des Orteils). Steinheil: Paris."},{"key":"ref_7","first-page":"259","article-title":"fiber die neurotische Muskelatrophie Charcot-Marie. Klinisch-genetische Studien. Zeitschriftfiir die gesamte Neurologie und","volume":"107","author":"Dawidenkow, S.","year":"1927","unstructured":"Dawidenkow, S. (1927). fiber die neurotische Muskelatrophie Charcot-Marie. Klinisch-genetische Studien. Zeitschriftfiir die gesamte Neurologie und Psychiatrie, 107, 259-320.","journal-title":"Psychiatrie"},{"key":"ref_8","first-page":"628","article-title":"Ober die scapulo-peroneal Amyotrophie. Zeitschriftfiir die gesamte Neurologie und","volume":"122","author":"Dawidenkow, S.","year":"1929","unstructured":"Dawidenkow, S. (1929). Ober die scapulo-peroneal Amyotrophie. Zeitschriftfiir die gesamte Neurologie und Psychiatrie, 122, 628-650.","journal-title":"Psychiatrie"},{"key":"ref_9","article-title":"Scapuloperoneal amyotrophy","author":"Dawidenkow, S.","year":"1939","unstructured":"Dawidenkow, S. (1939). Scapuloperoneal amyotrophy."},{"key":"ref_10","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1001\/archneur.1967.00470190018002","article-title":"'Myopathic' changes in chronically denervated muscle","volume":"16","author":"Drachman, D.B.; Murphy, S.R.; Nigam, M.P.; Hills, J.R.","year":"1967","unstructured":"Drachman, D. B., Murphy, S. R., Nigam, M. P., and Hills, J. R. (1967). 'Myopathic' changes in chronically denervated muscle. Archives of Neurology, 16, 14-24.","journal-title":"Archives of Neurology"},{"key":"ref_11","first-page":"564","article-title":"Ueber progressive muskelatrophie","volume":"8","author":"Eisenlohr, C.","year":"1889","unstructured":"Eisenlohr, C. (1889). Ueber progressive muskelatrophie. Neurologisches Zentralblatt, 8, 564-565.","journal-title":"Neurologisches Zentralblatt"},{"key":"ref_12","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1136\/jmg.3.2.92","article-title":"Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy","volume":"3","author":"Emery, A.E.H.","year":"1966","unstructured":"Emery, A. E. H. (1966). Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy. Journal of Medical Genietics, 3, 92-95.","journal-title":"Journal of Medical Genietics"},{"key":"ref_13","doi-asserted-by":"crossref","first-page":"338","DOI":"10.1136\/jnnp.29.4.338","article-title":"Unusual type of benign X-linked muscular dystrophy","volume":"29","author":"Emery, A.E.H.; Dreifuss, F.E.","year":"1966","unstructured":"Emery, A. E. H., and Dreifuss, F. E. (1966). Unusual type of benign X-linked muscular dystrophy. Journal ofNeurology, Neurosurgery, and Psychiatry, 29, 338-342.","journal-title":"Journal ofNeurology, Neurosurgery, and Psychiatry"},{"key":"ref_14","doi-asserted-by":"crossref","first-page":"129","DOI":"10.1001\/archneur.1968.00470320031003","article-title":"A spinal muscular atrophy with scapuloperoneal distribution","volume":"18","author":"Emery, E.S.; Fenichel, C.M.; Eng, G.","year":"1968","unstructured":"Emery, E. S., Fenichel, C. M., and Eng, G. (1968). A spinal muscular atrophy with scapuloperoneal distribution. Archives of Neurology, 18, 129-133.","journal-title":"Archives of Neurology"},{"key":"ref_15","first-page":"47","article-title":"A neuromuscular syndrome of scapulo-peroneal distribution","volume":"35","author":"Feigenbaum, J.A.; Munsat, T.L.","year":"1970","unstructured":"Feigenbaum, J. A., and Munsat, T. L. (1970). A neuromuscular syndrome of scapulo-peroneal distribution. Bulletin of the Los Angeles Neurological Society, 35, 47-57.","journal-title":"Bulletin of the Los Angeles Neurological Society"},{"key":"ref_16","first-page":"\"28","article-title":"Automatic measurement of the human electromyogram","volume":"178","author":"Fitch, P.; Willison, R.G.","year":"1965","unstructured":"Fitch, P., and Willison, R. G. (1965). Automatic measurement of the human electromyogram. Journal of PhYsiology, 178, 28-29P. Haase, G. R., and Shy, G. M. (1960). Pathological changes in muscle biopsies from patients with peroneal muscular atrophy. Brain, 83, 631-637.","journal-title":"Journal of PhYsiology; Pathological changes in muscle biopsies from patients with peroneal muscular atrophy"},{"key":"ref_17","first-page":"377","article-title":"Zur nosologischen Stellung des scapulo-peronealen Syndroms","volume":"183","author":"Hausmanowa-Petrusewicz, I.; Zielinska, S.","year":"1962","unstructured":"Hausmanowa-Petrusewicz, I., and Zielinska, S. (1962). Zur nosologischen Stellung des scapulo-peronealen Syndroms. Deutsche Zeitschriftfiir Nervenheilkunde, 183, 377-382.","journal-title":"Deutsche Zeitschriftfiir Nervenheilkunde"},{"key":"ref_18","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1093\/brain\/88.2.407","article-title":"Scapuloperoneal muscular atrophy","volume":"88","author":"Kaeser, H.E.","year":"1965","unstructured":"Kaeser, H. E. (1965). Scapuloperoneal muscular atrophy. Brain, 88, 407-418.","journal-title":"Brain"},{"key":"ref_19","first-page":"683","article-title":"Genetic aspects of neuromuscular disease","volume-title":"Disorders of Voluntary Muscle","author":"Kloepfer, H.W.; Emery, A.E.H.","year":"1969","unstructured":"Kloepfer, H. W., and Emery, A. E. H. (1969). Genetic aspects of neuromuscular disease. In Disorders of Voluntary Muscle, 2nd edn, pp. 683-712. Edited by J. N. Walton. Churchill: London.","edition":"2nd edn"},{"key":"ref_20","doi-asserted-by":"crossref","first-page":"1062","DOI":"10.1056\/NEJM196511112732002","article-title":"X-linked pseudohypertrophic muscular dystrophy with a late onset and slow progression","volume":"273","author":"Mabry, C.C.; Roeckel, I.E.; Munich, R.L.; Robertson, D.","year":"1965","unstructured":"Mabry, C. C., Roeckel, I. E., Munich, R. L., and Robertson, D. (1965). X-linked pseudohypertrophic muscular dystrophy with a late onset and slow progression. New, Eniglanid Journal of Medicinte, 273, 1062-1070.","journal-title":"New, Eniglanid Journal of Medicinte"},{"key":"ref_21","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1001\/archneur.1969.00480070019002","article-title":"Scapuloperoneal amyotrophy","volume":"20","author":"Meadows, J.C.; Marsden, C.D.","year":"1969","unstructured":"Meadows, J. C., and Marsden, C. D. (1969). Scapuloperoneal amyotrophy. Archives of Neurology, 20, 9-12.","journal-title":"Archives of Neurology"},{"key":"ref_22","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1007\/BF01669014","article-title":"fber einen hereditaren typus progressiver Muskeldystrophie","volume":"99","author":"Oransky, W.","year":"1927","unstructured":"Oransky, W. (1927). fber einen hereditaren typus progressiver Muskeldystrophie. Deutsche Zeitschrift fiir Nerteniheilkunde, 99, 147-155.","journal-title":"Deutsche Zeitschrift fiir Nerteniheilkunde"},{"key":"ref_23","doi-asserted-by":"crossref","first-page":"155","DOI":"10.1111\/j.1469-1809.1971.tb00276.x","article-title":"Colour blindness and the Duchenne-type muscular dystrophy","volume":"21","author":"Philip, U.; Walton, J.N.; Smith, C.A.B.","year":"1956","unstructured":"Philip, U., Walton, J. N., and Smith, C. A. B. (1956). Colour blindness and the Duchenne-type muscular dystrophy. Annals of Hunman Gentetics, 21, 155-158.","journal-title":"Annals of Hunman Gentetics"},{"key":"ref_24","doi-asserted-by":"crossref","first-page":"275","DOI":"10.1159\/000113669","article-title":"The differential diagnosis of the myogenic (facio)-scapulo-peroneal syndrome","volume":"1","author":"Ricker, K.; Mertens, H.G.","year":"1968","unstructured":"Ricker, K., and Mertens, H. G. (1968). The differential diagnosis of the myogenic (facio)-scapulo-peroneal syndrome. European Neurology, 1, 275-307.","journal-title":"European Neurology"},{"key":"ref_25","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1136\/jnnp.30.5.403","article-title":"Quantitative electromyography using automatic analysis: studies in heaithy subjects and in patients with primary muscle diseases","volume":"30","author":"Rose, A.L.; Willison, R.G.","year":"1967","unstructured":"Rose, A. L., and Willison, R. G. (1967). Quantitative electromyography using automatic analysis: studies in heaithy subjects and in patients with primary muscle diseases. Journal of Neurology, Neurosurgery, and Psychiatry, 30, 403-410.","journal-title":"Journal of Neurology, Neurosurgery, and Psychiatry"},{"key":"ref_26","doi-asserted-by":"crossref","first-page":"118","DOI":"10.1007\/BF00438809","article-title":"Spinal muscular atrophy of the scapulo-peroneal-type","volume":"109","author":"Schuchmann, L.","year":"1970","unstructured":"Schuchmann, L. (1970). Spinal muscular atrophy of the scapulo-peroneal-type. Zeitschrift fiur Kintderheilklnde, 109, 118-123.","journal-title":"Zeitschrift fiur Kintderheilklnde"},{"key":"ref_27","first-page":"547","article-title":"Zur nosologischen Stellung des sogenannten scapulo-peronealen Syndroms","volume":"175","author":"Seitz, D.","year":"1957","unstructured":"Seitz, D. (1957). Zur nosologischen Stellung des sogenannten scapulo-peronealen Syndroms. Deutsche Zeitschrift fiur Nerv7enheilkunde, 175, 547-552.","journal-title":"Deutsche Zeitschrift fiur Nerv7enheilkunde"},{"key":"ref_28","doi-asserted-by":"crossref","first-page":"451","DOI":"10.1001\/archneur.1969.00480110015001","article-title":"Mild and severe forms of X-linked muscular dystrophy","volume":"20","author":"Shaw, R.F.; Dreifuss, F.E.","year":"1969","unstructured":"Shaw, R. F., and Dreifuss, F. E. (1969). Mild and severe forms of X-linked muscular dystrophy. Archiv-es of Neurology, 20, 451-460.","journal-title":"Archiv-es of Neurology"},{"key":"ref_29","author":"Wilson, S.A.Kinnier","year":"1940","unstructured":"Wilson, S. A. Kinnier (1940). Neurology. Edited by A."},{"key":"ref_30","doi-asserted-by":"crossref","first-page":"968","DOI":"10.1542\/peds.29.6.968","article-title":"Intellectual function in childhood progressive muscular dystrophy","volume":"29","author":"Worden, D.K.; Vignos, P.J.","year":"1962","unstructured":"Worden, D. K., and Vignos, P. J. (1962). Intellectual function in childhood progressive muscular dystrophy. Pediatrics, 29, 968-977.","journal-title":"Pediatrics"}],"container-title":["Journal of Neurology, Neurosurgery & Psychiatry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jnnp.35.2.208","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,20]],"date-time":"2023-05-20T23:56:42Z","timestamp":1684627002000},"score":1,"resource":{"primary":{"URL":"https:\/\/jnnp.bmj.com\/lookup\/doi\/10.1136\/jnnp.35.2.208"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1972,4,1]]},"references-count":30,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1972,4,1]]}},"URL":"https:\/\/doi.org\/10.1136\/jnnp.35.2.208","relation":{},"ISSN":["0022-3050"],"issn-type":[{"value":"0022-3050","type":"print"}],"subject":[],"published":{"date-parts":[[1972,4,1]]}}}