Documents (100) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	14510914	Congenital hypothyroidism due to a new deletion in the sodium/iodide symporter protein. OBJECTIVE: I	1.88 KB	2015-11-18	15	1	2021-12-23
PubMed	15041272	A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation. Clinical, l	1.53 KB	2015-11-18	19	0	2021-12-23
PubMed	15096016	Pallidal stimulation: an alternative to pallidotomy? A resurgence of interest in the surgical treatm	1.33 KB	2021-12-23	8	0	2021-12-23
PubMed	15099351	Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia. Prop	1.09 KB	2015-11-18	12	0	2021-12-23
PubMed	15122708	Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotei	1.53 KB	2015-11-18	11	6	2021-12-23
PubMed	15188772	Severe reversible left ventricular systolic and diastolic dysfunction due to accidental iatrogenic e	830 Bytes	2017-09-04	10	0	2021-12-23
PubMed	15614572	Effects of the antidepressant trazodone, a 5-HT 2A/2C receptor antagonist, on dopamine-dependent beh	1.92 KB	2015-11-22	8	0	2021-12-23
PubMed	15623763	TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients. PURPOSE: T	1.89 KB	2015-11-18	13	0	2021-12-23
PubMed	15818664	Association of sporadic chondrocalcinosis with a -4-basepair G-to-A transition in the 5'-untranslate	2.28 KB	2015-11-19	11	0	2021-12-23
PubMed	15824163	No Evidence for BRAF as a melanoma/nevus susceptibility gene. Somatic mutations of BRAF have been id	1.75 KB	2015-11-19	12	0	2021-12-23