Results 191 to 200 of about 30,354 (250)

Portal diversion for inborn errors of metabolism: With special reference to glycogen storage disease, Type II hyperlipidemia, and juvenile Gaucher's disease [PDF]

, 1978
Putnam, CW, Starzl, TE
core  

Targeted NGS Revealed Pathogenic Mutation in a 13-Year-Old Patient with Homozygous Familial Hypercholesterolemia: A Case Report. [PDF]

Int J Mol Sci
Chamoieva AE, Mirmanova ZZ, Zhalbinova MR, Rakhimova SE, Daniyarov AZ, Kairov UY, Baigalkanova AI, Mukarov MA, Bekbossynova MS, Akilzhanova AR.   +9 more
europepmc   +1 more source

[Homozygous familial hypercholesterolemia (author's transl)].

Revista medica de Chile, 1980
F, Nervi, A, Arteaga, A, Maiz, J, Tocornal, M C, Severin   +4 more
openaire   +1 more source

Portasystemic shunting for metabolic disease [PDF]

, 1979
Benichou, J, Starzl, TE
core  

Lipoprotein apheresis: an established therapeutic modality for homozygous familial hypercholesterolemia patients refractory to PCSK9 inhibitors: a case report and literature review. [PDF]

Thromb J
Guan M, Wang H, Wang F, Liang S, Ling L, Wang B, Zhang L.   +6 more
europepmc   +1 more source

Pediatric Hepatology: A three-year experience with pediatric liver transplantation with cyclosporine and steroids [PDF]

, 1986
Gartner, JC, Iwatsuki, S, Malatack, JJ, Shaw, BW, Starzl, TE, Urbach, AH, Zitelli, BH   +6 more
core  

A machine-learning algorithm using claims data to identify patients with homozygous familial hypercholesterolemia. [PDF]

Sci Rep
Gu J, Epland M, Ma X, Park J, Sanchez RJ, Li Y.   +5 more
europepmc   +1 more source

Phenotypic homozygous familial hypercholesterolemia successfully treated with proprotein convertase subtilisin/kexin type 9 inhibitors. [PDF]

Clin Case Rep
Tani R, Matsunaga K, Toda Y, Inoue T, Fu HY, Minamino T.   +5 more
europepmc   +1 more source