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Daniel Landau

Research Profile

Concepts & Ideas

Living Beings

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Israel

Physiology

Mutation

Disorders

Chemicals & Drugs

Insulin Like Growth Factor I

Anatomy

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Chromosome Mapping

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Publications

TOP 3
Yuval Cavari; Daniel Landau; Tom Leibson; Shaul Sofer; Isaac Lazar
Organophosphate poisoning-induced acute renal failure.
Michael Volodarsky; Idan Cohen; Hagit Flusser; Daniel Landau; Yshaia Langer; Barak Markus; Ilan Shelef; Orna Staretz-Chacham; Ohad Birk
A deletion mutation in TMEM38B associated with autosomal recessive osteogenesis imperfecta.
Barak Markus; Ginat Narkis; Ruth Z Birk; Idan Cohen; Daniel Landau; Ohad Birk
Autosomal recessive lethal congenital contractural syndrome type 4 (LCCS4) caused by a mutation in MYBPC1.

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All Publications

2013: Yuval Cavari; Daniel Landau; Tom Leibson; Shaul Sofer; Isaac Lazar
Organophosphate poisoning-induced acute renal failure.
Pediatric emergency care 2013;29(5):646-7.
2013: Michael Volodarsky; Idan Cohen; Hagit Flusser; Daniel Landau; Yshaia Langer; Barak Markus; Ilan Shelef; Orna Staretz-Chacham; Ohad Birk
A deletion mutation in TMEM38B associated with autosomal recessive osteogenesis imperfecta.
Human mutation 2013;34(4):582-6.
2012: Barak Markus; Ginat Narkis; Ruth Z Birk; Idan Cohen; Daniel Landau; Ohad Birk
Autosomal recessive lethal congenital contractural syndrome type 4 (LCCS4) caused by a mutation in MYBPC1.
Human mutation 2012;33(10):1435-8.
2012: Hila Romi; Sara Sivan; Baruch Yerushalmi; Suliman Alkrinawi; Idan Cohen; Garry R Cutting; Reli Hershkovitz; Daniel Landau; Nitza Newman-Heiman; Rivka Ofir; Ohad Birk
Meconium ileus caused by mutations in GUCY2C, encoding the CFTR-activating guanylate cyclase 2C.
American journal of human genetics 2012;90(5):893-9.
2011: Ariel Troib; Jack F Youngren; Leonid Kachko; Daniel Landau; Ralph Rabkin; Yael Segev
The effects of type 1 IGF receptor inhibition in a mouse model of diabetic kidney disease.
Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society 2011;21(5):285-91.
2011: Daniel Landau; Derek LeRoith; Jaclyn Biada; Yu Chen; Yael Segev; Sumita Sood; Shoshanah Yakar; Ralph Rabkin
A marked deficiency in circulating and renal IGF-I peptide does not inhibit compensatory renal enlargement in uninephrectomized mice.
Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society 2011;21(5):279-84.
2010: Ruth Schreiber; Marie-Claire Gubler; Olivier Gribouval; Hanna Shalev; Daniel Landau
Inherited renal tubular dysgenesis may not be universally fatal.
Pediatric nephrology (Berlin, Germany) 2010;25(12):2531-4.
2010: Maya Feldshtein; Suliman Elkrinawi; Baruch Yerushalmi; Barak Marcus; Daniela Vullo; Hila Romi; Rivka Ofir; Daniel Landau; Sara Sivan; Claudiu T Supuran; Ohad Birk
Hyperchlorhidrosis caused by homozygous mutation in CA12, encoding carbonic anhydrase XII.
American journal of human genetics 2010;87(5):713-20.
2010: Arnon Broides; Michal S Maimon; Daniel Landau; Joseph Press; Matitiahu Lifshitz
Multiple hymenoptera stings in children: clinical and laboratory manifestations.
European journal of pediatrics 2010;169(10):1227-31.
2010: Daniel Landau; Hanna Shalev
[Childhood genetic renal diseases in southern Israel].
Harefuah 2010;149(3):180-5, 193.
2009: Yair Bar David; Jacob Urkin; Daniel Landau; Z Bar-David; D Pilpel
Voluntary dehydration among elementary school children residing in a hot arid environment.
Journal of human nutrition and dietetics : the official journal of the British Dietetic Association 2009;22(5):455-60.
2009: Daniel Landau; Rina Eshet; Ariel Troib; Yotam Gurman; Yu Chen; Ralph Rabkin; Yael Segev
Increased renal Akt/mTOR and MAPK signaling in type I diabetes in the absence of IGF type 1 receptor activation.
Endocrine 2009;36(1):126-34.
2008: Ramon Y Birnbaum; Daniel Landau; Khalil Elbedour; Rivka Ofir; Ohad Birk; Rivka Carmi
Deletion of the first pair of fibronectin type III repeats of the integrin beta-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients.
American journal of medical genetics. Part A 2008;146A(8):1063-6.
2008: Daniel Landau; Chen Chayat; Nili Zucker; Eli Golomb; Channa Yagil; Yoram Yagil; Yael Segev
Early blood pressure-independent cardiac changes in diabetic rats.
The Journal of endocrinology 2008;197(1):75-83.
2007: Ginat Narkis; Rivka Ofir; Esther Manor; Daniel Landau; Khalil Elbedour; Ohad Birk
Lethal congenital contractural syndrome type 2 (LCCS2) is caused by a mutation in ERBB3 (Her3), a modulator of the phosphatidylinositol-3-kinase/Akt pathway.
American journal of human genetics 2007;81(3):589-95.
2007: Ginat Narkis; Rivka Ofir; Daniel Landau; Esther Manor; Micha Volokita; Relly Hershkowitz; Khalil Elbedour; Ohad Birk
Lethal contractural syndrome type 3 (LCCS3) is caused by a mutation in PIP5K1C, which encodes PIPKI gamma of the phophatidylinsitol pathway.
American journal of human genetics 2007;81(3):530-9.
2007: Daniel Landau; Tal Oved; Dan Geiger; Luba Abizov; Hanna Shalev; Ruti Parvari
Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations.
Pediatric nephrology (Berlin, Germany) 2007;22(5):661-9.
2007: Ginat Narkis; Daniel Landau; Esther Manor; Rivka Ofir; Ohad Birk
Genetics of arthrogryposis: linkage analysis approach.
Clinical orthopaedics and related research 2007;456():30-5.
2006: Daniel Landau
Epithelial paracellular proteins in health and disease.
Current opinion in nephrology and hypertension 2006;15(4):425-9.
2006: Gal Finer; Hanna Shalev; Daniel Landau
Genetic kidney diseases in the pediatric population of southern Israel.
Pediatric nephrology (Berlin, Germany) 2006;21(7):910-6.
2005: Avraham Beigelman; Kyla-Anna Marks; Daniel Landau
Congenital isolated pleural effusion associated with obstructive uropathy.
The Israel Medical Association journal : IMAJ 2005;7(4):271-2.
2004: Daniel Landau
Potassium handling in health and disease: lessons from inherited tubulopathies.
Pediatric endocrinology reviews : PER 2004;2(2):203-8.
2004: Yael Segev; Renanah Eshet; Inessa Rivkis; Chen Hayat; Leonid Kachko; Moshe Phillip; Daniel Landau
Comparison between somatostatin analogues and ACE inhibitor in the NOD mouse model of diabetic kidney disease.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2004;19(12):3021-8.
2004: Ginat Narkis; Daniel Landau; Esther Manor; Khalil Elbedour; Anna Tzemach; Ma'ayan Fishelson; Dan Geiger; Rivka Ofir; Rivka Carmi; Ohad Birk
Homozygosity mapping of lethal congenital contractural syndrome type 2 (LCCS2) to a 6 cM interval on chromosome 12q13.
American journal of medical genetics. Part A 2004;130A(3):272-6.
2004: Gal Finer; Daniel Landau
Pathogenesis of urinary tract infections with normal female anatomy.
The Lancet infectious diseases 2004;4(10):631-5.
2004: Gal Finer; Ohad Birk; Daniel Landau
[Genetic and phenotypic aspects of autosomal recessive polycystic kidney disease in southern Israel].
Harefuah 2004;143(7):466-70, 552.
2004: Daniel Landau; D Cohen; Hanna Shalev; V Pinsk; B Yerushalmi; M Zeigler; Ohad Birk
A novel mutation in the SLC17A5 gene causing both severe and mild phenotypes of free sialic acid storage disease in one inbred Bedouin kindred.
Molecular genetics and metabolism 2004;82(2):167-72.
2004: Hanna Shalev; Igor Romanovsky; Nine V A M Knoers; Salomon Lupa; Daniel Landau
Bladder function impairment in aquaporin-2 defective nephrogenic diabetes insipidus.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2004;19(3):608-13.
2003: Hanna Shalev; Melly Ohali; Leonid Kachko; Daniel Landau
The neonatal variant of Bartter syndrome and deafness: preservation of renal function.
Pediatrics 2003;112(3 Pt 1):628-33.
2003: Daniel Landau; Eytan Israel; Inessa Rivkis; Leonid Kachko; Bieke F Schrijvers; Allan Flyvbjerg; Moshe Phillip; Yael Segev
The effect of growth hormone on the development of diabetic kidney disease in rats.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2003;18(4):694-702.
2003: Gal Finer; Hanna Shalev; Ohad Birk; Dalia Galron; Nikola Jeck; Levana Sinai-Treiman; Daniel Landau
Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome.
The Journal of pediatrics 2003;142(3):318-23.
2003: Daniel Landau; Anat Mishori-Dery; Reli Hershkovitz; Ginat Narkis; Khalil Elbedour; Rivka Carmi
A new autosomal recessive congenital contractural syndrome in an Israeli Bedouin kindred.
American journal of medical genetics. Part A 2003;117A(1):37-40.
2003: Reli Hershkovitz; OFFER EREZ; Eyal Sheiner; Daniel Landau; David Mankuta; Moshe Mazor
Elevated maternal mid-trimester chorionic gonadotropin > or =4 MoM is associated with fetal cerebral blood flow redistribution.
Acta obstetricia et gynecologica Scandinavica 2003;82(1):22-7.
2002: Roxanne Y Walder; Daniel Landau; Peter Meyer; Hanna Shalev; Maria Tsolia; Zvi Borochowitz; Melanie Barbara Boettger; Gretel E Beck; Richard K Englehardt; Rivka Carmi; Val C Sheffield
Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia.
Nature genetics 2002;31(2):171-4.
2001: Ruti Parvari; I Brodyansky; Orly Elpeleg; S Moses; Daniel Landau; Eli Hershkovitz
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.
American journal of human genetics 2001;69(4):869-75.
2001: Daniel Landau; Y Segev; M Afargan; A Silbergeld; Leonid Katchko; A Podshyvalov; M Phillip
A novel somatostatin analogue prevents early renal complications in the nonobese diabetic mouse.
Kidney international 2001;60(2):505-12.
2001: Ruti Parvari; Alla Shnaider; Anna Basok; Leonid Katchko; Z Borochovich; A Kanis; Daniel Landau
Clinical and genetic characterization of an autosomal dominant nephropathy.
American journal of medical genetics 2001;99(3):204-9.
2001: Daniel Landau; Hanna Shalev; G Levy-Finer; A Polonsky; Y Segev; Leonid Katchko
Familial hemolytic uremic syndrome associated with complement factor H deficiency.
The Journal of pediatrics 2001;138(3):412-7.
2001: Matityahu Lifshitz; Vladimir Gavrilov; A Galil; Daniel Landau
A four year survey of neonatal narcotic withdrawal: evaluation and treatment.
The Israel Medical Association journal : IMAJ 2001;3(1):17-20.
2000: Daniel Landau; D Tovbin; Hanna Shalev
Pediatric urolithiasis in southern Israel: the role of uricosuria.
Pediatric nephrology (Berlin, Germany) 2000;14(12):1105-10.
1999: L Ying; Y Katz; M Schlesinger; Rivka Carmi; Hanna Shalev; Neena B Haider; Gretel Beck; Val C Sheffield; Daniel Landau
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
American journal of human genetics 1999;65(6):1538-46.
1999: Daniel Landau; I Shelef; H Polacheck; K Marks; Gershon Holcberg
Perinatal vasoconstrictive renal insufficiency associated with maternal nimesulide use.
American journal of perinatology 1999;16(9):441-4.
1998: Neena B Haider; Rivka Carmi; Hanna Shalev; Val C Sheffield; Daniel Landau
A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mapping.
American journal of human genetics 1998;63(5):1404-10.
1998: Melly Ohali; Hanna Shalev; Menachem Schlesinger; Y Katz; Leonid Kachko; Rivka Carmi; S Sofer; Daniel Landau
Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H.
Pediatric nephrology (Berlin, Germany) 1998;12(8):619-24.
1998: Hanna Shalev; M Phillip; A Galil; Rivka Carmi; Daniel Landau
Clinical presentation and outcome in primary familial hypomagnesaemia.
Archives of disease in childhood 1998;78(2):127-30.
1998: T M H Brennan; Daniel Landau; Hanna Shalev; Fred Lamb; Brian C Schutte; Roxanne Y Walder; Allyn L Mark; Rivka Carmi; Val C Sheffield
Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.
American journal of human genetics 1998;62(2):355-61.
1997: Daniel Landau; K K Kher
Gentamicin-induced Bartter-like syndrome.
Pediatric nephrology (Berlin, Germany) 1997;11(6):737-40.
1997: Daniel Landau; J Mordechai; M Karplus; Rivka Carmi
Inheritance of familial congenital isolated anorectal malformations: case report and review.
American journal of medical genetics 1997;71(3):280-2.
1997: Y Segev; Daniel Landau; M Marbach; N Shehadeh; A Flyvbjerg; Moshe Phillip
Renal hypertrophy in hyperglycemic non-obese diabetic mice is associated with persistent renal accumulation of insulin-like growth factor I.
Journal of the American Society of Nephrology : JASN 1997;8(3):436-44.
1996: T Yermiahu; Hanna Shalev; Daniel Landau; Alexander Dvilansky
Protein C and protein S in pediatric nephrotic patients.
Sangre 1996;41(2):155-7.
1995: Daniel Landau; Hanna Shalev; M Ohaly; Rivka Carmi
Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder.
American journal of medical genetics 1995;59(4):454-9.
1995: Moshe Phillip; Daniel Landau; Y Segev; O Weiss; I Raz
Insulin-like growth factors (IGFs) and IGF-binding proteins in diabetic kidney disease.
Israel journal of medical sciences 1995;31(12):712-6.
1990: Hanna Shalev; Daniel Landau; A Gedalia; J Hershkovich
[Hypocalcemia associated with heart failure in infants].
Harefuah 1990;119(12):422-3.