D. Landau

发表

A marked deficiency in circulating and renal IGF-I peptide does not inhibit compensatory renal enlargement in uninephrectomized mice.

D. Leroith, S. Yakar, D. Landau, 2011, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2.

N. Gray, A. Wright, X. Shu, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidus.

D. Bichet, P. Deen, D. Landau, 2002, Journal of the American Society of Nephrology : JASN.

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

V. Sheffield, R. Carmi, D. Landau, 2002, Nature Genetics.

SOCS2 Silencing Improves Somatic Growth without Worsening Kidney Function in CKD

D. Landau, Yu Chen, Y. Segev, 2020, American Journal of Nephrology.

Chapter 13 – Effect of Nutritional Status and Changes in Protein Intake on Renal Function∗

D. Landau, R. Rabkin, 2013 .

Role of IGF-I in Type 2 diabetes: a focus on the mouse model

D. Landau, Y. Segev, 2008, Expert review of endocrinology & metabolism.

Growth hormone receptor antagonism prevents early renal changes in nonobese diabetic mice.

M. Phillip, D. Landau, Y. Segev, 1999, Journal of the American Society of Nephrology : JASN.

Pediatric chronic kidney disease rates in Southern Israel are higher than reported

D. Landau, H. Shalev, R. Schreiber, 2013, F1000Research.

Expression of insulin-like growth factor binding proteins in the rat kidney: effects of long-term diabetes.

C. Roberts, D. Leroith, D. Landau, 1995, Endocrinology.

Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations

D. Geiger, D. Landau, H. Shalev, 2007, Pediatric Nephrology.

Early blood pressure-independent cardiac changes in diabetic rats.

D. Landau, Y. Segev, E. Golomb, 2008, The Journal of endocrinology.

The neonatal variant of Bartter syndrome and deafness: preservation of renal function.

D. Landau, H. Shalev, L. Kachko, 2003, Pediatrics.

Involvement of the skeletal GH-IGF system in an experimental model of diabetes-induced growth retardation

M. Phillip, D. Landau, Y. Segev, 2002, Acta Diabetologica.

Renal tubulointerstitial injury from ureteral obstruction in the neonatal rat is attenuated by IGF-1.

D. Leroith, R. Chevalier, D. Landau, 2000, Kidney international.

Differential expression of renal growth hormone receptor and its binding protein in experimental diabetes mellitus.

S. Argov, C. Roberts, D. Leroith, 1998, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Endurance exercise and growth hormone improve bone formation in young and growth-retarded chronic kidney disease rats.

D. Landau, Y. Segev, R. Rabkin, 2016, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

The association between birth weight at term and long-term endocrine morbidity of the offspring*

D. Landau, E. Sheiner, I. Shoham-Vardi, 2019, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Epithelial paracellular proteins in health and disease

D. Landau, 2006, Current opinion in nephrology and hypertension.

Increased renal Akt/mTOR and MAPK signaling in type I diabetes in the absence of IGF type 1 receptor activation

D. Landau, Yu Chen, Y. Segev, 2009, Endocrine.

Renal hypertrophy in hyperglycemic non-obese diabetic mice is associated with persistent renal accumulation of insulin-like growth factor I.

M. Phillip, D. Landau, Y. Segev, 1997, Journal of the American Society of Nephrology : JASN.

Changes in facilitative glucose transporter messenger ribonucleic acid levels in the diabetic rat kidney.

D. Leroith, D. Landau, A. Flyvbjerg, 1997, Endocrinology.

Changes in Facilitative Glucose Transporter Messenger Ribonucleic Acid Levels in the Diabetic Rat Kidney.

D. Leroith, D. Landau, A. Flyvbjerg, 1997, Endocrinology.

Changes in the Growth Hormone-IGF-I Axis in Non-obese Diabetic Mice

M. Phillip, D. Landau, Y. Segev, 2000, International journal of experimental diabetes research.

The hypoxia inducible factor/erythropoietin (EPO)/EPO receptor pathway is disturbed in a rat model of chronic kidney disease related anemia

D. Landau, Y. Segev, Lital London, 2018, PloS one.

Prevalence of esophageal atresia among 18 international birth defects surveillance programs.

Miland N. Palmer, D. Tucker, M. Morgan, 2012, Birth defects research. Part A, Clinical and molecular teratology.

Clinical Approach to Proximal Renal Tubular Acidosis in Children.

D. Landau, Gal Finer, 2018, Advances in chronic kidney disease.

The effects of type 1 IGF receptor inhibition in a mouse model of diabetic kidney disease.

D. Landau, Y. Segev, R. Rabkin, 2011, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

A novel somatostatin analogue prevents early renal complications in the nonobese diabetic mouse.

M. Phillip, D. Landau, Y. Segev, 2001, Kidney international.

Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome.

O. Birk, D. Landau, H. Shalev, 2003, The Journal of pediatrics.

The role of growth hormone, insulin-like growth factors (IGFs), and IGF-binding proteins in experimental diabetic kidney disease.

D. Leroith, D. Landau, H. Grønbaek, 1995, Metabolism: clinical and experimental.

TRPM6 and Hypomagnesaemia/Hypocalcaemia

D. Landau, H. Shalev, 2014 .

Pathogenesis of urinary tract infections with normal female anatomy.

D. Landau, Gal Finer, 2004, The Lancet. Infectious diseases.

Persistent Pulmonary Hypertension of the Newborn Associated With Severe Congenital Anemia of Various Etiologies

D. Landau, H. Shalev, J. Kapelushnik, 2015, Journal of pediatric hematology/oncology.

Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder.

R. Carmi, D. Landau, H. Shalev, 1995, American journal of medical genetics.

Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome

G. Ariceta, D. Landau, S. Johnson, 2009, Pediatric nephrology (Berlin, West).

Epidemiology, Clinical Presentation, and Pathophysiology of Atypical and Recurrent Hemolytic Uremic Syndrome

H. Karch, G. Rizzoni, D. Landau, 2006, Seminars in thrombosis and hemostasis.

Genetic kidney diseases in the pediatric population of southern Israel

D. Landau, H. Shalev, Gal Finer, 2006, Pediatric Nephrology.

Current views on the diagnosis and management of hypokalaemia in children

D. Landau, J. Zieg, Lucie Gonsorčíková, 2016, Acta paediatrica.

Clinical presentation and outcome in primary familial hypomagnesaemia

M. Phillip, R. Carmi, D. Landau, 1998, Archives of disease in childhood.

The effect of growth hormone on the development of diabetic kidney disease in rats.

M. Phillip, D. Landau, Y. Segev, 2003, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Systemic and renal growth hormone–IGF1 axis involvement in a mouse model of type 2 diabetes

M. Phillip, D. Landau, Y. Segev, 2007, Diabetologia.

Epiphyseal growth plate growth hormone receptor signaling is decreased in chronic kidney disease-related growth retardation.

D. Landau, Y. Segev, R. Rabkin, 2013, Kidney international.

Febrile Proteinuria in Hospitalized Children: Characterization of Urinary Proteins

D. Landau, Y. Segev, Evgenia Gurevich, 2018, Front. Pediatr..

Amelia: A multi‐center descriptive epidemiologic study in a large dataset from the International Clearinghouse for Birth Defects Surveillance and Research, and overview of the literature

F. Bianchi, S. Bianca, G. Scarano, 2011, American journal of medical genetics. Part C, Seminars in medical genetics.

Systemic causes of non‐dermatologic chronic pruritus in the pediatric population and their management: An unexplored area

T. Miloh, D. Landau, G. Yosipovitch, 2021, Pediatric dermatology.

Impaired renal growth hormone JAK/STAT5 signaling in chronic kidney disease.

D. Landau, Y. Segev, R. Rabkin, 2014, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Clinical and genetic characterization of an autosomal dominant nephropathy.

D. Landau, R. Parvari, A. Shnaider, 2001, American journal of medical genetics.

D. Landau, 2006, Cellular and Molecular Life Sciences CMLS.

Differential effects on kidney and liver growth of a non-viral hGH-expression vector in hypophysectomized mice.

T. Jensen, M. Khamaisi, D. Landau, 2007, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Eculizumab Use for Kidney Transplantation in Patients With a Diagnosis of Atypical Hemolytic Uremic Syndrome

G. Ardissino, G. Ariceta, F. Schaefer, 2018, Kidney international reports.

Familial hemolytic uremic syndrome associated with complement factor H deficiency.

D. Landau, Y. Segev, H. Shalev, 2001, The Journal of pediatrics.

Bladder function impairment in aquaporin-2 defective nephrogenic diabetes insipidus.

D. Landau, N. Knoers, H. Shalev, 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

An audit analysis of a guideline for the investigation and initial therapy of diarrhea negative (atypical) hemolytic uremic syndrome

G. Ariceta, D. Landau, C. Langman, 2014, Pediatric Nephrology.

Urine metabolomics reveals novel physiologic functions of human aldehyde oxidase and provides biomarkers for typing xanthinuria

D. Landau, H. Shalev, D. Watson, 2012, Metabolomics.

Prevalence and Mortality in Children with Congenital Diaphragmatic Hernia: A Multi-Country Study.

A. Pierini, M. Morgan, E. Szabová, 2020, Annals of epidemiology.

Transient severe metastatic calcification in acute renal failure

D. Landau, H. Shalev, Hanna Krymko, 2006, Pediatric nephrology (Berlin, West).

Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H

R. Carmi, D. Landau, H. Shalev, 1998, Pediatric Nephrology.

Pediatric urolithiasis in southern Israel: the role of uricosuria

D. Landau, H. Shalev, D. Tovbin, 2000, Pediatric Nephrology.

A multi‐country study of prevalence and early childhood mortality among children with omphalocele

A. Pierini, M. Morgan, E. Szabová, 2020, Birth defects research.

Bladder exstrophy: An epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literature

S. Bianca, A. Pierini, G. Scarano, 2011, American journal of medical genetics. Part C, Seminars in medical genetics.

How valid are the rates of Down syndrome internationally? Findings from the International Clearinghouse for Birth Defects Surveillance and Research

Wladimir Wertelecki, Guido Cocchi, Pierpaolo Mastroiacovo, 2010, American journal of medical genetics. Part A.

SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome

G. Rutter, R. Zarivach, O. Birk, 2017, Brain : a journal of neurology.

Inheritance of familial congenital isolated anorectal malformations: case report and review.

R. Carmi, D. Landau, M. Karplus, 1997, American journal of medical genetics.

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

T. Strachan, B. Schermer, T. Benzing, 2003, Nature Genetics.

Trisomy 13 and 18—Prevalence and mortality—A multi‐registry population based analysis

A. Pierini, D. Tucker, M. Morgan, 2019, American journal of medical genetics. Part A.

Conjoined twins: A worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and Research

A. Pierini, G. Scarano, M. Morgan, 2011, American journal of medical genetics. Part C, Seminars in medical genetics.

A Down Syndrome Patient Treated by Peritoneal Dialysis

D. Landau, M. Hausmann, 2002, Nephron.

Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations

D. Geiger, D. Landau, H. Shalev, 2007, Pediatric Nephrology.

Eculizumab Safety: Five-Year Experience From the Global Atypical Hemolytic Uremic Syndrome Registry

D. Landau, E. Rondeau, S. Cataland, 2019, Kidney international reports.

Association between childhood nephrotic syndrome and hemophagocytic lymphohistiocytosis

I. Shelef, H. Tamary, D. Landau, 2013, Pediatric Nephrology.

Cyclopia: An epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research

F. Bianchi, G. Scarano, M. Morgan, 2011, American journal of medical genetics. Part C, Seminars in medical genetics.

Prenatal Diagnosis of a Rare Sonographic Appearance of Duodenal Atresia

D. Landau, R. Hershkovitz, G. Pariente, 2012, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

An international consensus approach to the management of atypical hemolytic uremic syndrome in children

R. Coppo, G. Ariceta, D. Landau, 2015, Pediatric Nephrology.

A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders.

G. Remuzzi, G. Rizzoni, D. Landau, 2006, Kidney international.

Protein C and protein S in pediatric nephrotic patients.

D. Landau, H. Shalev, T. Yermiahu, 1996, Sangre.

Protracted febrile myalgia in an afebrile child with familial Mediterranean fever

D. Landau, E. Ling, Hanna Krymko, 2014, International journal of rheumatic diseases.

Growth Hormone and IGF1 Actions in Kidney Development and Function

D. Landau, Y. Segev, Evgenia Gurevich, 2021, Cells.

Experimental modulation of Interleukin 1 shows its key role in chronic kidney disease progression and anemia

D. Landau, Y. Segev, Inbar Bandach, 2021, Scientific Reports.

Incidence of Impaired Kidney Function Among Adolescent Patients Hospitalized With Anorexia Nervosa

D. Landau, Evgenia Gurevich, Shelly Steiling, 2021, JAMA network open.

Case report: severe asymptomatic hyponatremia in Prader-Willi Syndrome

D. Landau, V. Gross‐Tsur, H. Hirsch, 2016, BMC Pediatrics.

Pediatric Tubulointerstitial Nephritis

L. Pape, D. Landau, Evgenia Gurevich, 2021, Pediatric Nephrology.

Accentuated hyperparathyroidism in type II Bartter syndrome

D. Landau, H. Shalev, Evgenia Gurevich, 2016, Pediatric Nephrology.

Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.

V. Sheffield, R. Carmi, D. Landau, 1999, American journal of human genetics.

Growth Hormone (GH) Hypersecretion and GH Receptor Resistance in Streptozotocin Diabetic Mice in Response to a GH Secretagogue

M. Phillip, D. Landau, Y. Segev, 2003, Experimental diabesity research.

Genetic renal disease classification by hormonal axes

D. Landau, Bar Rotem-Grunbaum, 2019, Pediatric Nephrology.

Comparison between somatostatin analogues and ACE inhibitor in the NOD mouse model of diabetic kidney disease.

M. Phillip, D. Landau, Y. Segev, 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Medically indicated late preterm delivery and its impact on perinatal morbidity and mortality: a retrospective population-based cohort study

D. Landau, O. Erez, M. Mazor, 2019, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Survival of infants born with esophageal atresia among 24 international birth defects surveillance programs

A. Pierini, M. Morgan, E. Szabová, 2021, Birth defects research.

Multiple hymenoptera stings in children: clinical and laboratory manifestations

D. Landau, J. Press, A. Broides, 2010, European Journal of Pediatrics.

A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mapping.

V. Sheffield, D. Landau, R. Carmi, 1998, American journal of human genetics.

Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.

V. Sheffield, R. Carmi, D. Landau, 1998, American journal of human genetics.

Perinatal Vasoconstrictive Renal Insufficiency Associated With Maternal Nimesulide Use

D. Landau, I. Shelef, D. Landau, 1999, American journal of perinatology.

Inherited renal tubular dysgenesis may not be universally fatal

O. Gribouval, M. Gubler, D. Landau, 2010, Pediatric Nephrology.

Gentamicin-induced Bartter-like syndrome

D. Landau, K. Kher, 1997, Pediatric Nephrology.

Brief report Gentamicin-induced Bartter-like syndrome

D. Landau, K. Kher, 1997 .

Phocomelia: A worldwide descriptive epidemiologic study in a large series of cases from the International Clearinghouse for Birth Defects Surveillance and Research, and overview of the literature

F. Bianchi, S. Bianca, G. Scarano, 2011, American journal of medical genetics. Part C, Seminars in medical genetics.

Bene ciary Effects of Colchicine on In ammation and Fibrosis in A Mouse Model of Chronic Kidney Disease

D. Landau, 2021 .

Organophosphate Poisoning-Induced Acute Renal Failure

D. Landau, S. Sofer, Tom Leibson, 2013, Pediatric emergency care.

Potassium handling in health and disease: lessons from inherited tubulopathies.

D. Landau, 2004, Pediatric endocrinology reviews : PER.

Bladder Exstrophy: An Epidemiologic Study From the International Clearinghouse for Birth Defects Surveillance and Research, and an Overview of the Literature

S. Bianca, A. Pierini, G. Scarano, 2011 .

Oligohydramnion, renal failure and no pulmonary hypoplasia in glomerulocystic kidney disease

D. Landau, H. Shalev, E. Maor, 2000, Pediatric Nephrology.

Comparison between somatostatin analogues and ACE inhibitor in the NOD mouse model of diabetic kidney disease.

M. Phillip, D. Landau, Y. Segev, 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Pathogenesis of urinary tract infections with normal female anatomy.

D. Landau, Gal Finer, 2004, The Lancet. Infectious diseases.

Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome

G. Ariceta, D. Landau, C. Licht, 2009, Pediatric Nephrology.