M. Tieder

发表

The effects of uremic serum and 3'-5' cyclic AMP on blastogenesis of normal lymphocytes.

A. Golik, J. Weissgarten, S. Peller, 1986, Thymus.

Induction of suppressor cells in normal lymphocytes by uremic serum.

J. Weissgarten, S. Peller, S. Kaufman, 1986, International archives of allergy and applied immunology.

VITAMIN D RESISTANT RICKETS WITH ALOPECIA: A FORM OF END ORGAN RESISTANCE TO 1,25 DIHYDROXY VITAMIN D

Z. Borochowitz, G. Bar-Joseph, D. Kohelet, 1981, Clinical endocrinology.

Direct measurement of TP/GFR: a simple and reliable parameter of renal phosphate handling.

B. Eisenstein, G. Alpert, H. Stark, 1986, Nephron.

Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene.

C. Langman, N. Roslin, K. Morgan, 2001, Journal of the American Society of Nephrology : JASN.

A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome.

D. Magen, K. Skorecki, S. Selig, 2010, The New England journal of medicine.

Effect of levamisole on chemotaxis of granulocytes from uremic patients.

A. Golik, J. Weissgarten, S. Peller, 1988, Nephron.

Therapy-Resistant Seizures in Pseudohypoparathyroidism - A Case Report

L. Pollak, C. Klein, A. Arlazoroff, 1995, Journal of pediatric endocrinology & metabolism : JPEM.

Maffucci's syndrome—The result of neural abnormalities? Evidence of mitogenic neurotransmitters present in enchondromas and soft tissue hemangiomas

D. Burshtein, N. Halperin, D. Robinson, 1994, Cancer.

Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation.

K. Fried, H. Krespin, M. Tieder, 1977, Journal of medical genetics.

SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis.

M. Bastepe, I. Sermet, J. Loredo-Osti, 2006, American journal of human genetics.

Hereditary hypophosphatemic rickets with hypercalciuria.

U. Liberman, D. Modai, R. Samuel, 1985, The New England journal of medicine.

The Weismann-Netter, Stuhl syndrome: A rare pediatric skeletal dysplasia

U. Alon, H. Manor, M. Tieder, 2005, Pediatric Radiology.

A practical approach to the treatment of burn shock in childhood.

H. Krespin, E. Vure, J. Shulman, 1982, Burns, including thermal injury.

Linear growth in patients with hypophosphatemic vitamin D-resistant rickets: influence of treatment regimen and parental height.

M. Tieder, S. Balsan, 1990, The Journal of pediatrics.

Osteomalacia in hereditary hypophosphatemic rickets with hypercalciuria: a correlative clinical-histomorphometric study.

U. Liberman, D. Gazit, I. Bab, 1991, Journal of Clinical Endocrinology and Metabolism.

Benign fibroepithelial polyps of the ureter and renal pelvis in childhood. Two case reports.

A. Zisman, A. Eidelman, M. Tieder, 1994, Scandinavian journal of urology and nephrology.

Elevated serum 1,25-dihydroxyvitamin D concentrations in siblings with primary Fanconi's syndrome.

U. Liberman, J. Weissgarten, D. Modai, 1988, The New England journal of medicine.

Detection and incidence of anomalies associated with hypospadias

A. Shalom, M. Westreich, T. Friedman, 2008, Pediatric Nephrology.

Renal abnormalities in the Bardet-Biedl syndrome.

M. Gubler, M. Lévy, M. Broyer, 1982, The International journal of pediatric nephrology.

[Familial form of idiopathic hypercalciuria with nanism, bone and renal involvement in children].

H. Stark, M. Tieder, 1979, Helvetica paediatrica acta.

"Idiopathic" hypercalciuria and hereditary hypophosphatemic rickets. Two phenotypical expressions of a common genetic defect.

J. Weissgarten, D. Modai, N. Cohen, 1987, The New England journal of medicine.

Spondyloepiphyseal dysplasia associated with progressive arthropathy

N. Halperin, D. Robinson, L. Copeliovitch, 1989, Archives of Orthopaedic and Trauma Surgery.

Pathophysiologic studies in idiopathic hypercalciuria presenting in childhood.

R. Shainkin-Kerstenbaum, H. Stark, M. Tieder, 1983, The International journal of pediatric nephrology.

A new kindred with hereditary hypophosphatemic rickets with hypercalciuria: implications for correct diagnosis and treatment.

U. Liberman, M. Tieder, I. Bab, 1992, Nephron.

Contents, Vol. 86, 1988

J. Denburg, V. Kurup, M. Chavance, 1988 .

Hereditary Hypophosphatemic Rickets with Hypercalciuria: Report of a New Kindred

I. Sermet-Gaudelus, G. Lenoir, M. Déchaux, 2001, Nephron.

Hyperoxaluria is not a cause of nephrocalcinosis in phosphate-treated patients with hereditary hypophosphatemic rickets.

B. Sela, H. Manor, M. Tieder, 1993, Nephron.

A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome.

D. Magen, K. Skorecki, S. Selig, 2010, The New England journal of medicine.

Hypercalciuria as a cause of persistent or recurrent haematuria.

M. Tieder, A. Litwin, Bella Eisenstein, 1988, Archives of disease in childhood.