نتائج البحث

A diagnostic support system based on pain drawings: binary and k-disease classification of EDS, GBS, FSHD, PROMM, and a control group with Pain2D

• Authors : D. Emmert; N. Szczypien; Tim T. A. Bender

Subjects: ORPHA: 269; ORPHA: 606; ORPHA: 2103

• Source: Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-13 (2023)

تفاصيل العنوان

A diagnostic support system based on pain drawings: binary and k-disease classification of EDS, GBS, FSHD, PROMM, and a control group with Pain2D.

• Authors : Emmert, D.^1,2 (AUTHOR); Szczypien, N.^3,4 (AUTHOR); Bender, Tim T. A.¹ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 3/28/2023, Vol. 18 Issue 1, p1-13. 13p.

تفاصيل العنوان

Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

• Authors : Kariminejad Ariana; Jones Kristi; Garcia Sixto

Subjects: Medicine

• Source: Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 46 (2011)

تفاصيل العنوان

Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation.

• Authors : Rohrbach M; Division of Metabolism, University Children's Hospital and Children's Research Centre, Zurich, Switzerland. ; Vandersteen A

Subjects: Ehlers-Danlos Syndrome/Ehlers-Danlos Syndrome/Ehlers-Danlos Syndrome/*pathology ; Kyphosis/Kyphosis/Kyphosis/*pathology ; Scoliosis/Scoliosis/Scoliosis/*pathology

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2011 Jun 23; Vol. 6, pp. 46. Date of Electronic Publication: 2011 Jun 23.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

تفاصيل العنوان

Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

• Authors : Carlo Marcelis; Gul Serdaroglu; Anthony Vandersteen ...

Subjects: Male; Connective Tissue Disorder; Muscle Hypotonia

• Source: Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 46 (2011)Orphanet Journal of Rare DiseasesOrphanet

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