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H Hurvitz

Showing results (51-60 of 58) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|April 23, 2005
Three novel mutations in POU1F1 in Israeli patients with combined pituitary hormone deficiencyG Gat-Yablonski, A Klar, D Hirsch, et al.
The Journal of Infection|September 1, 1992
Haemophilus influenzae type b purpura fulminans treated with hyperbaric oxygenS Dollberg, Z Nachum, A Klar, et al.
European Journal of Pediatrics|October 1, 1989
Glycogen storage disease, Fanconi nephropathy, abnormal galactose metabolism and mitochondrial myopathyH Hurvitz, O N Elpeleg, V Barash, et al.
The Journal of Pediatrics|June 1, 1996
Focal bacterial nephritis (lobar nephronia) in childrenA Klar, H Hurvitz, Y Berkun, et al.
Plastic and Reconstructive Surgery|January 1, 1995
Lipomatosis of the scalp and macrocephalyS N Lusthaus, P Benmeir, H Ashur, et al.
Journal of Pediatric Surgery|April 1, 1985
Mesenchymal hamartoma of the liver responsive to cyclophosphamide therapy: therapeutic approachA L Alkalay, A R Puri, J J Pomerance, et al.
Neurology|March 24, 2004
Rasmussen encephalitis with active inflammation and delayed seizures onsetI Korn-Lubetzki, C G Bien, J Bauer, et al.
The Journal of Clinical Investigation|December 26, 2001
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type IfB Schenk, T Imbach, C G Frank, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 23, 2005
Three novel mutations in POU1F1 in Israeli patients with combined pituitary hormone deficiencyG Gat-Yablonski, A Klar, D Hirsch, et al.
The Journal of Infection|September 1, 1992
Haemophilus influenzae type b purpura fulminans treated with hyperbaric oxygenS Dollberg, Z Nachum, A Klar, et al.
European Journal of Pediatrics|October 1, 1989
Glycogen storage disease, Fanconi nephropathy, abnormal galactose metabolism and mitochondrial myopathyH Hurvitz, O N Elpeleg, V Barash, et al.
The Journal of Pediatrics|June 1, 1996
Focal bacterial nephritis (lobar nephronia) in childrenA Klar, H Hurvitz, Y Berkun, et al.
Plastic and Reconstructive Surgery|January 1, 1995
Lipomatosis of the scalp and macrocephalyS N Lusthaus, P Benmeir, H Ashur, et al.
Journal of Pediatric Surgery|April 1, 1985
Mesenchymal hamartoma of the liver responsive to cyclophosphamide therapy: therapeutic approachA L Alkalay, A R Puri, J J Pomerance, et al.
Neurology|March 24, 2004
Rasmussen encephalitis with active inflammation and delayed seizures onsetI Korn-Lubetzki, C G Bien, J Bauer, et al.
The Journal of Clinical Investigation|December 26, 2001
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type IfB Schenk, T Imbach, C G Frank, et al.
Pageof 6