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1.
Gene mutations in chronic kidney disease patients with secondary hyperparathyroidism and Sagliker syndrome.
J Ren Nutr
; 25(2): 176-86, 2015 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-25701941
2.
A model for the noninvasive, habitat-inclusive estimation of upper limit abundance for synanthropes, exemplified by M. fascicularis.
Sci Adv
; 10(21): eadn5390, 2024 May 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-38787941
3.
International evaluation of unrecognizably uglifying human faces in late and severe secondary hyperparathyroidism in chronic kidney disease. Sagliker syndrome. A unique catastrophic entity, cytogenetic studies for chromosomal abnormalities, calcium-sensing receptor gene and GNAS1 mutations. Striking and promising missense mutations on the GNAS1 gene exons 1, 4, 10, 4.
J Ren Nutr
; 22(1): 157-61, 2012 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-22200434
4.
International study on Sagliker syndrome and uglifying human face appearance in severe and late secondary hyperparathyroidism in chronic kidney disease patients.
J Ren Nutr
; 18(1): 114-7, 2008 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-18089456
5.
Cephalometric evaluation of patients with Sagliker syndrome: uglifying human face appearance in severe and late secondary hyperparathyroidism in chronic renal failure patients.
J Ren Nutr
; 16(3): 229-32, 2006 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-16825025
6.
Neurologic manifestations in Sagliker syndrome: uglifying human face appearance in severe and late secondary hyperparathyroidism in chronic renal failure patients.
J Ren Nutr
; 16(3): 233-6, 2006 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-16825026
7.
The rate and significance of type 1/type 2 serum amyloid A protein gene polymorphisms in patients with ankylosing spondylitis and amyloidosis.
Amyloid
; 22(3): 207-8, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26300108
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