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Page 1
Genetic heterogeneity in Miyoshi-type distal muscular dystrophy.
Linssen WH, de Visser M, Notermans NC, Vreyling JP, Van Doorn PA, Wokke JH, Baas F, Bolhuis PA. Linssen WH, et al. Neuromuscul Disord. 1998 Jun;8(5):317-20. doi: 10.1016/s0960-8966(98)00020-0. Neuromuscul Disord. 1998. PMID: 9673985
Hyper-CK-aemia revisited.
Reijneveld JC, Notermans NC, Linssen WH, Bär PR, Wokke JH. Reijneveld JC, et al. Among authors: linssen wh. Neuromuscul Disord. 2001 Mar;11(2):163-4. doi: 10.1016/s0960-8966(00)00184-x. Neuromuscul Disord. 2001. PMID: 11257472 Review. No abstract available.
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients.
Ten Dam L, Frankhuizen WS, Linssen WHJP, Straathof CS, Niks EH, Faber K, Fock A, Kuks JB, Brusse E, de Coo R, Voermans N, Verrips A, Hoogendijk JE, van der Pol L, Westra D, de Visser M, van der Kooi AJ, Ginjaar I. Ten Dam L, et al. Among authors: linssen whjp. Clin Genet. 2019 Aug;96(2):126-133. doi: 10.1111/cge.13544. Epub 2019 May 6. Clin Genet. 2019. PMID: 30919934
Benign prognosis in idiopathic hyper-CK-emia.
Reijneveld JC, Notermans NC, Linssen WH, Wokke JH. Reijneveld JC, et al. Among authors: linssen wh. Muscle Nerve. 2000 Apr;23(4):575-9. doi: 10.1002/(sici)1097-4598(200004)23:4<575::aid-mus17>3.0.co;2-5. Muscle Nerve. 2000. PMID: 10716769
65 results