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M Tieder

Showing results (11-20 of 40) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|July 1, 1995
Therapy-resistant seizures in pseudohypoparathyroidism. A case reportL Pollak, C Klein, M Tieder, et al.
Acta Orthopaedica Scandinavica|August 1, 1991
Spondyloenchondrodysplasia. A rare cause of short-trunk syndromeD Robinson, M Tieder, L Copeliovitch, et al.
Archives of Disease in Childhood|March 1, 1988
Hypercalciuria as a cause of persistent or recurrent haematuriaH Stark, M Tieder, B Eisenstein, et al.
Archives Francaises De Pediatrie|May 1, 1976
[Salt-losing syndrome in newborn infants with hyperaldosteronism. Presenting a sensitivity to mineralocorticoids. Pseudohypoaldosteronism]M Tieder, E Vure, Y Gulboa, et al.
Pediatric Radiology|January 1, 1995
The Weismann-Netter, Stuhl syndrome: a rare pediatric skeletal dysplasiaM Tieder, H Manor, J Peshin, et al.
Nephron|January 1, 1992
A new kindred with hereditary hypophosphatemic rickets with hypercalciuria: implications for correct diagnosis and treatmentM Tieder, R Arie, I Bab, et al.
Nephron|January 1, 1986
Direct measurement of TP/GFR: a simple and reliable parameter of renal phosphate handlingH Stark, B Eisenstein, M Tieder, et al.
Helvetica Paediatrica Acta|July 1, 1975
The management of benign renal tumors of infancy. Case report of a congenital mesoblastic nephroma (leiomyomatous hamartoma)A Eidelman, J Sibi, E Vure, et al.
Harefuah|March 1, 1981
[Congenital ectodermal dysplasia]S Beer, E Heyman, C Sarnat, et al.
International Surgery|January 1, 1982
Spontaneous rupture of renal allograft: case reportD Modai, D Gabizon, B Siegal, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 1, 1995
Therapy-resistant seizures in pseudohypoparathyroidism. A case reportL Pollak, C Klein, M Tieder, et al.
Acta Orthopaedica Scandinavica|August 1, 1991
Spondyloenchondrodysplasia. A rare cause of short-trunk syndromeD Robinson, M Tieder, L Copeliovitch, et al.
Archives of Disease in Childhood|March 1, 1988
Hypercalciuria as a cause of persistent or recurrent haematuriaH Stark, M Tieder, B Eisenstein, et al.
Archives Francaises De Pediatrie|May 1, 1976
[Salt-losing syndrome in newborn infants with hyperaldosteronism. Presenting a sensitivity to mineralocorticoids. Pseudohypoaldosteronism]M Tieder, E Vure, Y Gulboa, et al.
Pediatric Radiology|January 1, 1995
The Weismann-Netter, Stuhl syndrome: a rare pediatric skeletal dysplasiaM Tieder, H Manor, J Peshin, et al.
Nephron|January 1, 1992
A new kindred with hereditary hypophosphatemic rickets with hypercalciuria: implications for correct diagnosis and treatmentM Tieder, R Arie, I Bab, et al.
Nephron|January 1, 1986
Direct measurement of TP/GFR: a simple and reliable parameter of renal phosphate handlingH Stark, B Eisenstein, M Tieder, et al.
Helvetica Paediatrica Acta|July 1, 1975
The management of benign renal tumors of infancy. Case report of a congenital mesoblastic nephroma (leiomyomatous hamartoma)A Eidelman, J Sibi, E Vure, et al.
Harefuah|March 1, 1981
[Congenital ectodermal dysplasia]S Beer, E Heyman, C Sarnat, et al.
International Surgery|January 1, 1982
Spontaneous rupture of renal allograft: case reportD Modai, D Gabizon, B Siegal, et al.
Pageof 4