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201. Occurrence of Congenital Heart Defects in Relation to Maternal Multivitamin Use.

202. 5, 10-Methylenetetrahydrofolate Reductase Gene Variants and Congenital Anomalies: A HuGE Review.

203. Case-control study of self reported genitourinary infections and risk of gastroschisis: findings from the national birth defects prevention study, 1997-2003.

204. Fostering International Collaboration in Birth Defects Research and Prevention: A Perspective From the International Clearinghouse for Birth Defects Surveillance and Research.

206. Vitamin A and cardiac outflow tract defects.

210. Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings

211. Maternal Smoking and Congenital Heart Defects, National Birth Defects Prevention Study, 1997-2011.

212. Case-control study of self reported genitourinary infections and risk of gastroschisis: findings from the national birth defects prevention study, 1997-2003

214. Seeking causes: Classifying and evaluating congenital heart defects in etiologic studiesThe authors have indicated that they have no financial relationships to this article to disclose.The findings and conclusions in this report are those of the author(s) and do not necessarily represent the views of the Centers for Disease Control and Prevention.

215. Prenatally diagnosed congenital heart disease: the cost of maternal care.

217. Join World Birth Defects Day.

218. International retrospective cohort study of neural tube defects in relation to folic acid recommendations: are the recommendations working?

221. Early Childhood Inpatient Costs of Critical Congenital Heart Disease.

222. Clinical and biochemical outcomes of patients with medium-chain acyl-CoA dehydrogenase deficiency.

223. Brief Report: Pediatrician Perspectives Regarding Genetic Evaluations of Children with Autism Spectrum Disorder.

224. Associations between maternal periconceptional exposure to secondhand tobacco smoke and major birth defects.

226. International Undiagnosed Diseases Programs (UDPs): components and outcomes.

227. Congenital heart defects after maternal fever.

228. Lack of periconceptional vitamins or supplements that contain folic acid and diabetes mellitus-associated birth defects.

229. Maternal nutrition and gastroschisis: findings from the National Birth Defects Prevention Study.

230. Maternal use of bupropion and risk for congenital heart defects.

231. Association between prepregnancy body mass index and congenital heart defects.

232. Diabetes mellitus and birth defects.

233. (Mis)classifying limb deficiencies: A reply to “Academicians are more likely to share each other's toothbrush than each other's nomenclature (Cohen, 1982)”

234. ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy.

235. International retrospective cohort study of neural tube defects in relation to folic acid recommendations: are the recommendations working?

236. A novel RAD51 variant resulting in Fanconi anemia identified in an infant with multiple congenital anomalies.

237. Heterozygous NOTCH1 Variants Cause CNS Immune Activation and Microangiopathy.

238. Pathogenic variants of sphingomyelin synthase SMS2 disrupt lip.

241. Does Maternal Exposure to Secondhand Tobacco Smoke During Pregnancy Increase the Risk for Preterm or Small-for-Gestational Age Birth?

242. Improving maternal folate status to prevent infant neural tube defects: working group conclusions and a framework for action.

243. Maternal Exposure to Nitrogen Dioxide, Intake of Methyl Nutrients, and Congenital Heart Defects in Offspring.

245. Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling.

246. Effect of dietary lysine restriction and arginine supplementation in two patients with pyridoxine-dependent epilepsy.

247. Evidence-Based Treatment of Guanidinoacetate Methyltransferase (GAMT) Deficiency.

248. Glutaric acidemia Type 1: Outcomes before and after expanded newborn screening

249. Cardiomyopathy and carnitine deficiency

250. Delineation of the 9q31 deletion syndrome: Genomic microarray characterization of two patients with overlapping deletions

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