Back to Search
FULGENCIO DEL CASTILLO, M.D.
M.D.
Developmental - Behavioral Pediatrics Physician
NPI: 1881692291Individual
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
C177174(CA)
Developmental - Behavioral Pediatrics PhysicianPrimary
Pediatrics — Developmental - Behavioral Pediatrics
Code: 2080P0006X
C177174(CA)
Research & Publications (20)
Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNA(Ser(UCN)) gene.
PMID 12471220·J Med Genet·2002
8-other
Construction and characterization of mutations at codon 751 of the Escherichia coli gyrB gene that confer resistance to the antimicrobial peptide microcin B17 and alter the activity of DNA gyrase.
PMID 11222617·J Bacteriol·2001
8-other
Secretion of the Escherichia coli K-12 SheA hemolysin is independent of its cytolytic activity.
PMID 11731136·FEMS Microbiol Lett·2001
8-other
Characterization of the genes encoding the SheA haemolysin in Escherichia coli O157:H7 and Shigella flexneri 2a.
PMID 10865950·Res Microbiol·2000
8-other
Successful treatment of childhood cutaneous leishmaniasis with liposomal amphotericin B: report of two cases.
PMID 19656844·J Trop Pediatr·2010
5-case
Endoscopic medial maxillectomy as a procedure of choice to treat inverted papillomas.
PMID 19037823·Acta Otolaryngol·2009
8-other
Coronary involvement in infants with Kawasaki disease treated with intravenous gamma-globulin.
PMID 17917769·Pediatr Cardiol·2008
8-other
[Acute otitis media in the era of pneumococcal vaccination].
PMID 19094865·Enferm Infecc Microbiol Clin·2008
6-review
Visual evoked responses in children with tuberculosis treated with ethambutol.
PMID 17195719·Pediatr Infect Dis J·2007
8-other
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy.
PMID 16804542·Nat Genet·2006
7-preclinical
Marburgvirus genomics and association with a large hemorrhagic fever outbreak in Angola.
PMID 16775337·J Virol·2006
8-other
Cerebrospinal fluid leucocyte counts in healthy neonates.
PMID 16418305·Arch Dis Child Fetal Neonatal Ed·2006
6-review
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment.
PMID 15994881·J Med Genet·2005
4-observational
[Fiberoptic bronchoscopy in childhood endobronchial tuberculosis].
PMID 15456586·An Pediatr (Barc)·2004
8-other
Cerebrospinal fluid beta 2-microglobulin values in perinatally acquired cytomegalovirus infection.
PMID 15361739·Pediatr Infect Dis J·2004
5-case
Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF).
PMID 14635104·Hum Mutat·2003
8-other
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study.
PMID 14571368·Am J Hum Genet·2003
4-observational
Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss.
PMID 12920080·J Med Genet·2003
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 710 LAWRENCE EXPY DEPT 190
SANTA CLARA, CA 95051 - Phone
- (408) 851-1240
Quick Facts
- NPI
- 1881692291
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile