Search research articles
Contact Us
Filters
Showing results (1-10 of 23) with videos related to
Page
of 3
Sort By:
Pediatric Neurology
|
January 22, 1998
Type IV 3-methylglutaconic (3-MGC) aciduria: a new case presenting with hepatic dysfunction
E Broide, O Elpeleg, E Lahat
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
June 28, 2018
Fetal exome sequencing: yield and limitations in a tertiary referral center
H Daum, V Meiner, O Elpeleg, et al.
The Pediatric Infectious Disease Journal
|
February 27, 2001
Dichloroacetate treatment for severe refractory metabolic acidosis during neonatal sepsis
S Arnon, I Litmanovits, R Regev, et al.
Harefuah
|
December 15, 1988
[Results of screening for organic aciduria in Israel]
O Elpeleg, N Amir, H Hurvitz, et al.
Annals of Neurology
|
January 1, 1993
3-Methylglutaconic aciduria in "optic atrophy plus"
H Costeff, O Elpeleg, N Apter, et al.
American Journal of Human Genetics
|
October 23, 2001
Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews
Y Anikster, R Kleta, A Shaag, et al.
Prenatal Diagnosis
|
November 1, 1988
Measurement of 3-hydroxy-3-methylglutaryl-CoA lyase activity in amniotic cells and in chorionic villi
V Barash, O Elpeleg, R Sheffer, et al.
American Journal of Human Genetics
|
August 29, 2001
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease
R Parvari, I Brodyansky, O Elpeleg, et al.
JIMD Reports
|
February 11, 2015
Hepatic Copper Accumulation: A Novel Feature in Transient Infantile Liver Failure Due to TRMU Mutations?
Z Grover, P Lewindon, A Clousten, et al.
Nature Genetics
|
November 1, 2001
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
A Saada, A Shaag, H Mandel, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
Pediatric Neurology
|
January 22, 1998
Type IV 3-methylglutaconic (3-MGC) aciduria: a new case presenting with hepatic dysfunction
E Broide, O Elpeleg, E Lahat
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
June 28, 2018
Fetal exome sequencing: yield and limitations in a tertiary referral center
H Daum, V Meiner, O Elpeleg, et al.
The Pediatric Infectious Disease Journal
|
February 27, 2001
Dichloroacetate treatment for severe refractory metabolic acidosis during neonatal sepsis
S Arnon, I Litmanovits, R Regev, et al.
Harefuah
|
December 15, 1988
[Results of screening for organic aciduria in Israel]
O Elpeleg, N Amir, H Hurvitz, et al.
Annals of Neurology
|
January 1, 1993
3-Methylglutaconic aciduria in "optic atrophy plus"
H Costeff, O Elpeleg, N Apter, et al.
American Journal of Human Genetics
|
October 23, 2001
Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews
Y Anikster, R Kleta, A Shaag, et al.
Prenatal Diagnosis
|
November 1, 1988
Measurement of 3-hydroxy-3-methylglutaryl-CoA lyase activity in amniotic cells and in chorionic villi
V Barash, O Elpeleg, R Sheffer, et al.
American Journal of Human Genetics
|
August 29, 2001
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease
R Parvari, I Brodyansky, O Elpeleg, et al.
JIMD Reports
|
February 11, 2015
Hepatic Copper Accumulation: A Novel Feature in Transient Infantile Liver Failure Due to TRMU Mutations?
Z Grover, P Lewindon, A Clousten, et al.
Nature Genetics
|
November 1, 2001
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
A Saada, A Shaag, H Mandel, et al.
Page
of 3