D. Katznelson

发表

Transient exocrine pancreatic insufficiency in infancy.

A. Jonas, S. Avigad, A. Diver-Haber, 1983, The Journal of pediatrics.

Lungfunction ininfants withcystic fibrosis

S. Godfrey, E. Bar-Yishay, C. Beardsmore, 1988 .

Lung function in infants with cystic fibrosis.

S. Godfrey, E. Bar-Yishay, C. Beardsmore, 1988, Thorax.

Pathological confirmation of cystic fibrosis in the fetus following prenatal diagnosis.

J. Opitz, A. Ornoy, B. Caspi, 1987, American journal of medical genetics.

Pheochromocytoma and hydralazine-induced myocardial ischaemia in a 14-year-old boy

J. Sack, E. Friedman, D. Katznelson, 1986, European Journal of Pediatrics.

Lundh meal: a single non-invasive challenge test for evaluation of exocrine and endocrine pancreatic function in cystic fibrosis patients

J. Sack, A. Blank, A. Augarten, 1999, International journal of clinical & laboratory research.

Pigment deposition in the reticuloendothelial system after fat emulsion infusion.

B. Cohen, D. Katznelson, J. Passwell, 1976, Archives of disease in childhood.

The gene encoding vasoactive intestinal peptide is located on human chromosome 6p21→6qter

C. Croce, K. Huebner, I. Gozes, 1987, Human Genetics.

Prediction of mortality and timing of referral for lung transplantation in cystic fibrosis patients

E. Picard, H. Blau, J. Rivlin, 2001, Pediatric transplantation.

COHERENCE AS A MEASURE OF FUTURE TIME PERSPECTIVE IN CHILDREN AND ITS RELATIONSHIP TO DELAY OF GRATIFICATION AND SOCIAL CLASS

D. Shmotkin, D. Katznelson, J. Lomranz, 1983 .

Persistent cough a forme-fruste of asthma.

D. Katznelson, S. Benzaray, Y. Yahav, 1982, European journal of respiratory diseases.

Performance of High-Yielding Dairy Cows Fed Liquid Whey

Y. Pinchasov, A. Hasdai, R. Volcani, 1982 .

Congenital Malformations in Four Siblings of a Mother Taking Anticonvulsant Drugs

D. Katznelson, M. Hertz, R. Goodman, 1976 .

Disturbed fat absorption following infectious gastroenteritis in children.

A. Jonas, S. Avigad, A. Diver-Haber, 1979, The Journal of pediatrics.

Extensive infantile retroperitoneal haemangioma causing severe retroperitoneal and gastrointestinal bleeding associated with haemangioma of the thigh. A syndrome?

E. Shahar, A. Jónás, A. Jonas, 1980, Australian paediatric journal.

Familial glioblastoma multiforme without neurofibromatosis.

D. Katznelson, J. Chemke, G. Zucker, 1985, American journal of medical genetics.

Angiographic features of arterial lesions in neurofibromatosis.

Y. Itzchak, A. Jónás, D. Katznelson, 1974, The American journal of roentgenology, radium therapy, and nuclear medicine.

[Relapsing fever in the area of Kefar-Saba].

U. Brook, D. Katznelson, S. Gross, 1976, Harefuah.

Polyneuritis following BCG re-vaccination

J. Sack, D. Katznelson, S. Gross, 1982, Postgraduate medical journal.

Liver cirrhosis and portal hypertension in cystic fibrosis

D. Vilozni, D. Modan-Moses, A. Augarten, 2002, European journal of gastroenterology & hepatology.

Growth and Puberty Arrest due to Prolactinoma

J. Sack, R. Tadmor, D. Katznelson, 1984, Acta paediatrica Scandinavica.

Tuberculosis of the middle ear in an infant.

G. Leventon, D. Katznelson, S. Davidson, 1989, Archives of otolaryngology--head & neck surgery.

Familial Clustering of Tonsillectomies and Adenoidectomies

D. Katznelson, S. Gross, 1980, Clinical pediatrics.

Long-term treatment of diabetes insipidus with a synthetic analog of vasopressin during pregnancy.

J. Sack, Y. Frenkel, D. Katznelson, 1980, Israel journal of medical sciences.

A syndrome characterized by congenital ichthyosis with atrophy, mental retardation, dwarfism, and generalized aminoaciduria.

B. Cohen, A. Szeinberg, D. Katznelson, 1973, The Journal of pediatrics.

Hemoglobin A1 and pancreatic beta cell function in cystic fibrosis.

J. Sack, A. Eshkol, T. Bistritzer, 1983, Israel journal of medical sciences.

The significance of sweat Cl/Na ratio in patients with borderline sweat test

Eitan Kerem, B. Kerem, E. Kerem, 1995, Pediatric pulmonology.

On the complexity of the pulmonary microbiology in cystic fibrosis: thoughts of a clinician.

D. Katznelson, 2006, The Israel Medical Association journal : IMAJ.

Serum CA 19–9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat tests

B. Kerem, H. Blau, E. Kerem, 2003, Clinical and Experimental Medicine.

Fosfomycin in the treatment of cystic fibrosis

E. Rubinstein, D. Katznelson, Y. Yahav, 1984, European Journal of Clinical Microbiology.

Sex reassignment in a girl with 11 beta-hydroxylase deficiency.

J. Sack, A. Eshkol, T. Bistritzer, 1984, Israel journal of medical sciences.

INCREASED INTRACRANIAL PRESSURE IN CYSTIC FIBROSIS

D. Katznelson, 1978, Acta paediatrica Scandinavica.

Serum lipase levels pre and post Landh meal: Evaluation of exocrine pancreatic status in cystic fibrosis

B. Kerem, J. Sack, A. Lusky, 1998, International journal of clinical & laboratory research.

Congenital hypoaldosteronism. Thirteen year follow-up in identical twins.

B. Lunenfeld, J. Sack, Z. Kraiem, 1979, Hormone research.

DETECTION OF CYSTIC-FIBROSIS GENOTYPES

H. Blau, J. Sack, D. Katznelson, 1983, The Lancet.

Heat inactivation of plasma hydrolases as a means of discriminating between the genotypes in cystic fibrosis: the experience in Israel.

J. Sack, M. Frass, D. Katznelson, 1981, Israel journal of medical sciences.

HEAT INACTIVATION OF PLASMA HYDROLASES IN CYSTIC FIBROSIS

J. Sack, M. Frass, D. Katznelson, 1980, The Lancet.

Cystic fibrosis in Israel: clinical and genetic aspects.

D. Katznelson, M. Ben-Yishay, 1978, Israel journal of medical sciences.

Liver cirrhosis and portal hypertension in cystic fibrosis

D. Vilozni, D. Modan-Moses, A. Augarten, 2003, European journal of gastroenterology & hepatology.