Search research articles
Contact Us
Filters
Showing results (1-10 of 76) with videos related to
Page
of 8
Sort By:
Developmental Medicine and Child Neurology
|
September 4, 2022
Common data elements and minimum data sets in cerebral palsy: Start small to grow big
Klaus Dieterich
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 20, 2022
PNS or not PNS, a dilemma of the post-genomic era in neurogenic developmental disorders
Klaus Dieterich
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 5, 2019
Classification of arthrogryposis
Judith G Hall, Eva Kimber, Klaus Dieterich
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 15, 2019
Central nervous system involvement in arthrogryposis multiplex congenita: Overview of causes, diagnosis, and care
Klaus Dieterich, Eva Kimber, Judith G Hall
Orthopaedics & Traumatology, Surgery & Research : OTSR
|
December 15, 2020
Amyoplasia and distal arthrogryposis
Jacques Griffet, Klaus Dieterich, Véronique Bourg, et al.
Neurology
|
March 27, 2019
Author response: Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Shenhao Dai, Klaus Dieterich, Marie Jaeger, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
May 20, 2026
Spinal Involvement in a Pediatric and Adult Cohort of Patients With Arthrogryposis Multiplex Congenita
Alicia Mom, Véronique Bourg, Shenhao Dai, et al.
Neurology
|
April 8, 2018
Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Shenhao Dai, Klaus Dieterich, Marie Jaeger, et al.
American Journal of Medical Genetics. Part A
|
December 12, 2017
"Lowe syndrome: A particularly severe phenotype without clinical kidney involvement"
Ebtesam Abdalla, Ahmed El-Beheiry, Klaus Dieterich, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 2, 2019
The diagnostic workup in a patient with AMC: Overview of the clinical evaluation and paraclinical analyses with review of the literature
Klaus Dieterich, Pauline Le Tanno, Eva Kimber, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 76) with videos related to
Sort By:
Page
of 8
Developmental Medicine and Child Neurology
|
September 4, 2022
Common data elements and minimum data sets in cerebral palsy: Start small to grow big
Klaus Dieterich
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 20, 2022
PNS or not PNS, a dilemma of the post-genomic era in neurogenic developmental disorders
Klaus Dieterich
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 5, 2019
Classification of arthrogryposis
Judith G Hall, Eva Kimber, Klaus Dieterich
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 15, 2019
Central nervous system involvement in arthrogryposis multiplex congenita: Overview of causes, diagnosis, and care
Klaus Dieterich, Eva Kimber, Judith G Hall
Orthopaedics & Traumatology, Surgery & Research : OTSR
|
December 15, 2020
Amyoplasia and distal arthrogryposis
Jacques Griffet, Klaus Dieterich, Véronique Bourg, et al.
Neurology
|
March 27, 2019
Author response: Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Shenhao Dai, Klaus Dieterich, Marie Jaeger, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
May 20, 2026
Spinal Involvement in a Pediatric and Adult Cohort of Patients With Arthrogryposis Multiplex Congenita
Alicia Mom, Véronique Bourg, Shenhao Dai, et al.
Neurology
|
April 8, 2018
Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Shenhao Dai, Klaus Dieterich, Marie Jaeger, et al.
American Journal of Medical Genetics. Part A
|
December 12, 2017
"Lowe syndrome: A particularly severe phenotype without clinical kidney involvement"
Ebtesam Abdalla, Ahmed El-Beheiry, Klaus Dieterich, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 2, 2019
The diagnostic workup in a patient with AMC: Overview of the clinical evaluation and paraclinical analyses with review of the literature
Klaus Dieterich, Pauline Le Tanno, Eva Kimber, et al.
Page
of 8