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T N Willig

Showing results (11-20 of 22) with videos related to

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American Journal of Physical Medicine & Rehabilitation|January 1, 1995
Correlation of flexion contractures with upper extremity function and pain for spinal muscular atrophy and congenital myopathy patientsT N Willig, J R Bach, M J Rouffet, et al.
Ear, Nose, & Throat Journal|January 1, 1994
Swallowing disorders in muscular diseases: functional assessment and indications of cricopharyngeal myotomyJ L St Guily, S Périé, T N Willig, et al.
Seminars in Neurology|March 1, 1995
Evaluation and management of dysphagiaC Gilardeau, M S Kazandjian, J R Bach, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1993
[Cardiac involvement in certain muscular diseases. Apropos of 216 cases]J Monségu, D Duboc, L Freychet, et al.
Magnetic Resonance Imaging|January 1, 1997
Body composition determined with MR in patients with Duchenne muscular dystrophy, spinal muscular atrophy, and normal subjectsA Leroy-Willig, T N Willig, M C Henry-Feugeas, et al.
Blood|January 3, 2001
Lutheran blood group glycoprotein and its newly characterized mouse homologue specifically bind alpha5 chain-containing human laminin with high affinityS F Parsons, G Lee, F A Spring, et al.
Nature Genetics|February 13, 1999
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemiaN Draptchinskaia, P Gustavsson, B Andersson, et al.
Blood|December 3, 1998
High adenosine deaminase level among healthy probands of Diamond Blackfan anemia (DBA) cosegregates with the DBA gene region on chromosome 19q13. The DBA Working Group of Société d'Immunologie Pédiatrique (SHIP)T N Willig, J L Pérignon, P Gustavsson, et al.
Blood|December 10, 1999
Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expressionT N Willig, N Draptchinskaia, I Dianzani, et al.
Pediatric Research|December 14, 1999
Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 Diamond-Blackfan anemia patients. DBA group of Société d'Hématologie et d'Immunologie Pédiatrique (SHIP), Gesellshaft für Pädiatrische Onkologie und Hämatologie (GPOH), and the European Society for Pediatric Hematology and Immunology (ESPHI)T N Willig, C M Niemeyer, T Leblanc, et al.
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Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
American Journal of Physical Medicine & Rehabilitation|January 1, 1995
Correlation of flexion contractures with upper extremity function and pain for spinal muscular atrophy and congenital myopathy patientsT N Willig, J R Bach, M J Rouffet, et al.
Ear, Nose, & Throat Journal|January 1, 1994
Swallowing disorders in muscular diseases: functional assessment and indications of cricopharyngeal myotomyJ L St Guily, S Périé, T N Willig, et al.
Seminars in Neurology|March 1, 1995
Evaluation and management of dysphagiaC Gilardeau, M S Kazandjian, J R Bach, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1993
[Cardiac involvement in certain muscular diseases. Apropos of 216 cases]J Monségu, D Duboc, L Freychet, et al.
Magnetic Resonance Imaging|January 1, 1997
Body composition determined with MR in patients with Duchenne muscular dystrophy, spinal muscular atrophy, and normal subjectsA Leroy-Willig, T N Willig, M C Henry-Feugeas, et al.
Blood|January 3, 2001
Lutheran blood group glycoprotein and its newly characterized mouse homologue specifically bind alpha5 chain-containing human laminin with high affinityS F Parsons, G Lee, F A Spring, et al.
Nature Genetics|February 13, 1999
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemiaN Draptchinskaia, P Gustavsson, B Andersson, et al.
Blood|December 3, 1998
High adenosine deaminase level among healthy probands of Diamond Blackfan anemia (DBA) cosegregates with the DBA gene region on chromosome 19q13. The DBA Working Group of Société d'Immunologie Pédiatrique (SHIP)T N Willig, J L Pérignon, P Gustavsson, et al.
Blood|December 10, 1999
Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expressionT N Willig, N Draptchinskaia, I Dianzani, et al.
Pediatric Research|December 14, 1999
Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 Diamond-Blackfan anemia patients. DBA group of Société d'Hématologie et d'Immunologie Pédiatrique (SHIP), Gesellshaft für Pädiatrische Onkologie und Hämatologie (GPOH), and the European Society for Pediatric Hematology and Immunology (ESPHI)T N Willig, C M Niemeyer, T Leblanc, et al.
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