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1.
Efficacy and Safety of Eculizumab in Pediatric Patients Affected by Shiga Toxin-Related Hemolytic and Uremic Syndrome: A Randomized, Placebo-Controlled Trial.
J Am Soc Nephrol
; 34(9): 1561-1573, 2023 09 01.
Artículo
Inglés
| MEDLINE | ID: mdl-37303085
2.
Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease.
Kidney Int
; 99(3): 737-749, 2021 03.
Artículo
Inglés
| MEDLINE | ID: mdl-32750455
3.
SNORD116 and growth hormone therapy impact IGFBP7 in Prader-Willi syndrome.
Genet Med
; 23(9): 1664-1672, 2021 09.
Artículo
Inglés
| MEDLINE | ID: mdl-34040195
4.
Comparison between pediatric and adult adipose mesenchymal stromal cells.
Cytotherapy
; 19(3): 395-407, 2017 03.
Artículo
Inglés
| MEDLINE | ID: mdl-28040462
5.
Bone defects in LPA receptor genetically modified mice.
Biochim Biophys Acta
; 1831(1): 93-8, 2013 Jan.
Artículo
Inglés
| MEDLINE | ID: mdl-22867754
6.
Peritraumatic distress predicts prolonged grief disorder symptom severity after the death of a parent in children and adolescents.
Eur J Psychotraumatol
; 12(1): 1936916, 2021.
Artículo
Inglés
| MEDLINE | ID: mdl-34249245
7.
Ghrelin uses the GHS-R1a/Gi/cAMP pathway and induces differentiation only in mature osteoblasts. This ghrelin pathway is impaired in AIS patients.
Biochem Biophys Rep
; 24: 100782, 2020 Dec.
Artículo
Inglés
| MEDLINE | ID: mdl-32984555
8.
The ANTENATAL multicentre study to predict postnatal renal outcome in fetuses with posterior urethral valves: objectives and design.
Clin Kidney J
; 13(3): 371-379, 2020 Jun.
Artículo
Inglés
| MEDLINE | ID: mdl-32699617
9.
Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial.
Lancet Diabetes Endocrinol
; 7(9): 695-706, 2019 09.
Artículo
Inglés
| MEDLINE | ID: mdl-31377265
10.
Hyperghrelinemia precedes obesity in Prader-Willi syndrome.
J Clin Endocrinol Metab
; 93(7): 2800-5, 2008 Jul.
Artículo
Inglés
| MEDLINE | ID: mdl-18460565
11.
Feasibility, Safety and Accuracy of Echocardiography-Fluoroscopy Imaging Fusion During Percutaneous Atrial Septal Defect Closure in Children.
J Am Soc Echocardiogr
; 31(11): 1229-1237, 2018 11.
Artículo
Inglés
| MEDLINE | ID: mdl-30219347
12.
Systems biology combining human- and animal-data miRNA and mRNA data identifies new targets in ureteropelvic junction obstruction.
BMC Syst Biol
; 11(1): 31, 2017 03 01.
Artículo
Inglés
| MEDLINE | ID: mdl-28249581
13.
Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome.
Eur J Hum Genet
; 23(2): 252-5, 2015 Feb.
Artículo
Inglés
| MEDLINE | ID: mdl-24916642
14.
Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age and FBN1 Genotype.
J Bone Miner Res
; 30(8): 1369-76, 2015 Aug.
Artículo
Inglés
| MEDLINE | ID: mdl-25656438
15.
Absence of the lysophosphatidic acid receptor LPA1 results in abnormal bone development and decreased bone mass.
Bone
; 49(3): 395-403, 2011 Sep.
Artículo
Inglés
| MEDLINE | ID: mdl-21569876
16.
Functional effects of PTPN11 (SHP2) mutations causing LEOPARD syndrome on epidermal growth factor-induced phosphoinositide 3-kinase/AKT/glycogen synthase kinase 3beta signaling.
Mol Cell Biol
; 30(10): 2498-507, 2010 May.
Artículo
Inglés
| MEDLINE | ID: mdl-20308328
17.
LEPROT and LEPROTL1 cooperatively decrease hepatic growth hormone action in mice.
J Clin Invest
; 119(12): 3830-8, 2009 Dec.
Artículo
Inglés
| MEDLINE | ID: mdl-19907080
18.
Human dental follicle cells acquire cementoblast features under stimulation by BMP-2/-7 and enamel matrix derivatives (EMD) in vitro.
Cell Tissue Res
; 329(2): 283-94, 2007 Aug.
Artículo
Inglés
| MEDLINE | ID: mdl-17443352
19.
Hyperghrelinemia is a common feature of Prader-Willi syndrome and pituitary stalk interruption: a pathophysiological hypothesis.
Horm Res
; 62(1): 49-54, 2004.
Artículo
Inglés
| MEDLINE | ID: mdl-15192277
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