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H Mocan

Showing results (61-70 of 70) with videos related to

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Journal of Child Psychology and Psychiatry, and Allied Disciplines|February 1, 1996
Relationships between serum free fatty acids and zinc, and attention deficit hyperactivity disorder: a research noteM Bekaroğlu, Y Aslan, Y Gedik, et al.
The Turkish Journal of Pediatrics|January 20, 1998
Absorption of iron from grape-molasses and ferrous sulfate: a comparative study in normal subjects and subjects with iron deficiency anemiaY Aslan, E Erduran, H Mocan, et al.
International Urology and Nephrology|January 1, 1995
Effect of essential amino acid supplementation in acute renal failureM Z Mocan, H Mocan, M N Gacar, et al.
Polish Journal of Pharmacology|March 1, 1995
The role of calcium channel entry blocker in experimental ischemia-reperfusion-induced intestinal injuryH Mocan, Y Gedik, E Erduran, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|April 20, 1999
The effect of ATP-MgCl2 on lipid peroxidation in ischemic and reperfused rabbit kidneyH Mocan, H Saruhan, M K Arslan, et al.
Acta Paediatrica Scandinavica|November 1, 1989
A prospective study of children with first acute symptomatic E. coli urinary tract infection. Early 99mtechnetium dimercaptosuccinic acid scan appearancesD M Tappin, A V Murphy, H Mocan, et al.
Scottish Medical Journal|October 1, 1989
Serratia marcescens outbreak in a paediatric oncology unit traced to contaminated chlorhexidineT A McAllister, C E Lucas, H Mocan, et al.
Journal of Medical Genetics|February 5, 2003
A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosisK J Borthwick, N Kandemir, R Topaloglu, et al.
Nature Genetics|January 23, 1999
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafnessF E Karet, K E Finberg, R D Nelson, et al.
Journal of Medical Genetics|November 5, 2002
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing lossE H Stover, K J Borthwick, C Bavalia, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|February 1, 1996
Relationships between serum free fatty acids and zinc, and attention deficit hyperactivity disorder: a research noteM Bekaroğlu, Y Aslan, Y Gedik, et al.
The Turkish Journal of Pediatrics|January 20, 1998
Absorption of iron from grape-molasses and ferrous sulfate: a comparative study in normal subjects and subjects with iron deficiency anemiaY Aslan, E Erduran, H Mocan, et al.
International Urology and Nephrology|January 1, 1995
Effect of essential amino acid supplementation in acute renal failureM Z Mocan, H Mocan, M N Gacar, et al.
Polish Journal of Pharmacology|March 1, 1995
The role of calcium channel entry blocker in experimental ischemia-reperfusion-induced intestinal injuryH Mocan, Y Gedik, E Erduran, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|April 20, 1999
The effect of ATP-MgCl2 on lipid peroxidation in ischemic and reperfused rabbit kidneyH Mocan, H Saruhan, M K Arslan, et al.
Acta Paediatrica Scandinavica|November 1, 1989
A prospective study of children with first acute symptomatic E. coli urinary tract infection. Early 99mtechnetium dimercaptosuccinic acid scan appearancesD M Tappin, A V Murphy, H Mocan, et al.
Scottish Medical Journal|October 1, 1989
Serratia marcescens outbreak in a paediatric oncology unit traced to contaminated chlorhexidineT A McAllister, C E Lucas, H Mocan, et al.
Journal of Medical Genetics|February 5, 2003
A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosisK J Borthwick, N Kandemir, R Topaloglu, et al.
Nature Genetics|January 23, 1999
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafnessF E Karet, K E Finberg, R D Nelson, et al.
Journal of Medical Genetics|November 5, 2002
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing lossE H Stover, K J Borthwick, C Bavalia, et al.
Pageof 7