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Clinical Pediatrics|June 4, 2002
Mediastinal tumors in children: a single institution experienceE Freud, J Ben-Ari, T Schonfeld, et al.
Optics Express|May 5, 2019
Improving techniques for diagnostics of laser pulses by compact representationsP Sidorenko, A Dikopoltsev, T Zahavy, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|January 22, 2013
[Irinotecan plus temozolomide in refractory or relapsed pediatric solid tumors]C Hernández-Marqués, A Lassaletta-Atienza, A Ruiz Hernández, et al.
Neurologia|October 17, 2021
Impulsiveness in children with attention-deficit/hyperactivity disorder after an 8-week intervention with the Mediterranean diet and/or omega-3 fatty acids: a randomised clinical trialI San Mauro Martin, S Sanz Rojo, L González Cosano, et al.
Neurologia|December 30, 2019
Impulsiveness in children with attention-deficit/hyperactivity disorder after an 8-week intervention with the Mediterranean diet and/or omega-3 fatty acids: A randomised clinical trialI San Mauro Martin, S Sanz Rojo, L González Cosano, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|December 1, 1990
Adjunctive therapy with bromocriptine in Parkinson's diseaseJ A Temlett, A Ming, M Saling, et al.
Genomics|February 10, 1995
The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia geneS A Slaugenhaupt, A Blumenfeld, C B Liebert, et al.
Protein Expression and Purification|June 23, 2009
High yield expression of biologically active recombinant full length human tuftelin protein in baculovirus-infected insect cellsB Shay, Y Gruenbaum-Cohen, A S Tucker, et al.
Nature Genetics|June 1, 1993
Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosisA Blumenfeld, S A Slaugenhaupt, F B Axelrod, et al.
Oncogene|February 6, 1997
Frequent loss of chromosome 14 in atypical and malignant meningioma: identification of a putative 'tumor progression' locusA G Menon, J L Rutter, J P von Sattel, et al.
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