Results 251 to 260 of about 57,313 (306)

Neurofibromatosis type 1 accompanied by acromelanoma: A case report. [PDF]

Medicine (Baltimore)
Dong S, Zhang M, Zhang Y, Ma Y, Mou Y.
europepmc   +1 more source

Novel CHKB Mutation Causing Megaconial Congenital Muscular Dystrophy: A Case Report from India. [PDF]

Ann Indian Acad Neurol
Gowda VK, Srinivasan VM, Krishnanada V, Sathyakumar R, Mahadevan A.   +4 more
europepmc   +1 more source

First Iranian Family with a Novel Missense Variant in <i>MYO9B</i> Gene Causing Charcot-Marie-Tooth Disease. [PDF]

Arch Iran Med
Beheshtian M, Mozaffarpour Nouri M, Ahangari F, Makvand M, Salmani B, Kariminejad A, Najmabadi H, Nafissi S.   +7 more
europepmc   +1 more source

Reassessing the Mechanisms of PLN-R14del Cardiomyopathy: From Calcium Dysregulation to S/ER Malformation. [PDF]

JACC Basic Transl Sci
Stege NM, de Boer RA, Makarewich CA, van der Meer P, Silljé HHW.   +4 more
europepmc   +1 more source

"Cyclic nucleotides in plants: from obscure messengers to central regulators". [PDF]

Front Plant Sci
Świeżawska-Boniecka B, Szmidt-Jaworska A.   +1 more
europepmc   +1 more source

RAS mutation identifies a poor prognostic molecular subtype of therapy-related myeloid neoplasm. [PDF]

Blood Adv
Kok CH, Al-Kali A, Thomas D, He R, Kutyna MM, Alkhateeb H, Lim K, Saliba AN, Toop C, Matin A, Scott H, Gangat N, Brown A, Mangaonkar A, Hahn CN, Begna K, Hung K, Greipp P, Hogan WJ, Patnaik M, Shah M, Hiwase DK.   +21 more
europepmc   +1 more source

Thyrotoxic periodic Paralysis With hypoxemia: A case report and a comprehensive review. [PDF]

Radiol Case Rep
Song W, Gu D, Ji B, Guo Q, Liu C.
europepmc   +1 more source