sonoma

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source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	74953	Amniotic fluid alpha-fetoprotein elevation with fetal omphalocele and a possible mechanism for its occurrence. Prenatal diagnosis of genetic disease and congenital malformations has become a major are	786 Bytes	2015-12-04	10	57	2022-02-22
PubMed	7130957	[Acetylcholinesterase of amniotic fluid: application to prenatal diagnosis of neural tube closing defects. I. Quantitative tests]. Acetylcholinesterase (AChE) in amniotic fluid from 165 normal pregnan	1.39 KB	2015-12-07	4	72	2021-11-14
PubMed	2443614	[Prenatal diagnosis of 4 cases of spina bifida in mothers treated with valproate]. The potential risk of spina bifida (SB) after fetal exposure to Valproate led the authors to apply the following prot	785 Bytes	2016-01-17	7	27	2021-08-10
PubMed	3356011	P-450 enzyme induction by 5-ethyl-5-phenylhydantoin and 5,5-diethylhydantoin, analogues of barbiturate tumor promoters phenobarbital and barbital, and promotion of liver and thyroid carcinogenesis ini	1.97 KB	2015-03-12	2	80	2021-08-10
PubMed	2453005	Second-trimester maternal serum alpha-fetoprotein levels in pregnancies associated with gastroschisis and omphalocele. This population-based study analyzes maternal serum alpha-fetoprotein (MSAFP) dis	1.08 KB	2016-01-15	3	40	2021-11-01
PubMed	3133336	Effects of phenobarbital and carbazole on carcinogenesis of the lung, thyroid, kidney, and bladder of rats pretreated with N-bis(2-hydroxypropyl)nitrosamine. Studies were made on potential modifying e	868 Bytes	2015-03-12	2	31	2021-08-10
PubMed	3165727	Linkage studies of Best's macular dystrophy. Genetic linkage studies are presented for nine kindreds with Best's vitelliform macular dystrophy (BVMD). This condition is an autosomal dominant macular d	1.17 KB	2015-11-27	4	41	2021-09-30
PubMed	3137195	Dose-dependent induction of liver and thyroid neoplastic lesions by short-term administration of 2-amino-3-methylimidazo[4,5-f]quinoline combined with partial hepatectomy followed by phenobarbital or	1.24 KB	2015-12-05	2	59	2021-08-10
PubMed	3180550	Alkaptonuria and ochronosis in three siblings. Ascorbic acid treatment monitored by urinary HGA excretion. Patients with alkaptonuria lack homogentisate 1,2-dioxygenase leading to retention of homogen	876 Bytes	2015-11-27	11	32	2021-10-19
PubMed	2196279	Two unrelated patients with familial hyperproinsulinemia due to a mutation substituting histidine for arginine at position 65 in the proinsulin molecule: identification of the mutation by direct seque	1.59 KB	2015-11-26	4	106	2021-11-17