- 3390/ijms20184548. PMC 6770289. PMID 31540302. Aoki,
Masashi (March 5, 2015). "
Dysferlinopathy". GeneReviews. PMID 20301480. Benarroch, Louise; Bonne, Gisèle; Rivier...
-
inherited myopathies may have
secondary myositis,
including calpainopathy,
dysferlinopathy,
facioscapulohumeral muscular dystrophy, dystrophinopathy, and LMNA-****ociated...
-
Distal Myopathy (DM). A
reduction or
absence of dysferlin,
termed dysferlinopathy,
usually becomes apparent in the
third or
fourth decade of life and...
- myopathy, the DMPK gene in
myotonic dystrophy, and
genes related to
dysferlinopathy and Parkinson's disease.
These genes could serve as
targets for gene...
- 1590/S0004-282X2003000600011. PMID 14762596. Aoki,
Masashi (1
January 1993). "
Dysferlinopathy". GeneReviews. PMID 20301480.
Retrieved 10 May 2016. Saperstein, DS;...
-
Dyserythropoietic anemia,
congenital type 3 Dy****ecutive
syndrome Dysferlinopathy Dysfibrinogenemia,
familial Dysfibrinogenemia,
acquired Dysgerminoma...
- by Dr. Pradhan.
Diamond on
quadriceps sign: The sign is
related to
dysferlinopathy. A
clinical study of 31
patients revealed that the
patients with the...
-
Haraldur was born with a
genetic muscular dystrophy disease known as
dysferlinopathy that
forced him to use a
wheelchair at the age of 25. His
parents were...
-
dysferlin causes a
group of
muscular dystrophies called dysferlinopathies.
Dysferlinopathies include limb-girdle
muscular dystrophy (LGMD) 2B, Miyoshi...
- "Aquaporin-4
expression is
severely reduced in
human sarcoglycanopathies and
dysferlinopathies". Cell Cycle. 7 (14): 2199–207. doi:10.4161/cc.7.14.6272. PMID 18641458...
