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kw.\*:("Kidney agenesis")

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Results 1 to 25 of 65

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Islet1 Deletion Causes Kidney Agenesis and Hydroureter Resembling CAKUTKAKU, Yusuke; OHMORI, Tomoko; KUDO, Kuniko et al.Journal of the American Society of Nephrology. 2013, Vol 24, Num 8, pp 1242-1249, issn 1046-6673, 8 p.Article

Case 94 : Uterus didelphys with obstructing hemivaginal septum and ipsilateral renal agenesisMADUREIRA, Antonio J; MARIZ, Carlos M; BERNARDES, Joao C et al.Radiology. 2006, Vol 239, Num 2, pp 602-606, issn 0033-8419, 5 p.Article

Plumbing in the embryo : developmental defects of the urinary tractsUETANI, N; BOUCHARD, M.Clinical genetics. 2009, Vol 75, Num 4, pp 307-317, issn 0009-9163, 11 p.Article

Heterotopic gastric mucosa in gallbladder associated with kidney agenesis and congenital hip dysplasiaCÖL, C; BORAN, C; TURKELI, V et al.Acta Clinica Belgica. 2007, Vol 62, Num 2, pp 120-122, issn 0001-5512, 3 p.Article

FREM1 Mutations Cause Bifid Nose, Renal Agenesis, and Anorectal Malformations SyndromeALAZAMI, Anas M; SHAHEEN, Ranad; ALZAHRANI, Fatema et al.American journal of human genetics. 2009, Vol 85, Num 3, pp 414-418, issn 0002-9297, 5 p.Article

Complete unilateral leg duplication with ipsilateral renal agenesisLILJE, Christian; FINGER, Leron J; ASCUITTO, Robert J et al.Acta paediatrica (Oslo). 2007, Vol 96, Num 3, pp 464-466, issn 0803-5253, 3 p.Article

A New Syndrome of Microtia With Unilateral Renal Agenesis and Short StatureOKAY CAGLAYAN, Ahmet; STEVENS, Servi J. C; ALBRECHTS, Jozefa C. M et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 8, pp 1837-1840, issn 1552-4825, 4 p.Article

Bilateral Eventration of the Diaphragm with Malrotation and Unilateral Renal AgenesisSHARMA, Shyam B; DEBNATH, Pinaki R; TRIPATHI, Rakesh et al.Indian journal of pediatrics. 2007, Vol 74, Num 5, pp 503-504, issn 0019-5456, 2 p.Article

Sprouty1 Haploinsufficiency Prevents Renal Agenesis in a Model of Fraser SyndromePITERA, Jolanta E; WOOLF, Adrian S; ALBERT BASSON, M et al.Journal of the American Society of Nephrology. 2012, Vol 23, Num 11, pp 1790-1796, issn 1046-6673, 7 p.Article

RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defectsJEANPIERRE, Cécile; MACE, Guillaume; LOGET, Philippe et al.Journal of medical genetics. 2011, Vol 48, Num 7, pp 497-504, issn 0022-2593, 8 p.Article

Loss of Sprouty1 Rescues Renal Agenesis Caused by Ret MutationROZEN, Esteban J; SCHMIDT, Hagen; DOLCET, Xavier et al.Journal of the American Society of Nephrology. 2009, Vol 20, Num 2, pp 255-259, issn 1046-6673, 5 p.Article

FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME WITH RENAL AGENESIS AND PATENT DUCTUS ARTERIOSUSTATAR AKSOY, H; ERAS, Z; KADIOGLU SIMSEK, G et al.Genetic counseling. 2013, Vol 24, Num 3, pp 351-355, issn 1015-8146, 5 p.Article

False diagnosis of renal agenesis on fetal MRISGRO, M; SHAH, V; BAROZZINO, T et al.Ultrasound in obstetrics & gynecology. 2005, Vol 25, Num 2, pp 197-200, issn 0960-7692, 4 p.Article

Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesisGRIBOUVAL, Olivier; GONZALES, Marie; LAUBE, Guido et al.Nature genetics. 2005, Vol 37, Num 9, pp 964-968, issn 1061-4036, 5 p.Article

Herlyn-Werner-Wunderlich Syndrome Consisting of Uterine Didelphys, Obstructed Hemivagina and Ipsilateral Renal Agenesis in a NewbornWU, Tsung-Hsin; WU, Trang-Tiau; NG, Yan-Yan et al.Pediatrics & neonatology (Print). 2012, Vol 53, Num 1, pp 68-71, issn 1875-9572, 4 p.Article

Evaluating Compensatory Hypertrophy: A Growth Curve Specific for Solitary Functioning KidneysKILL, Aaron; SALAMI, Simpa; ROSEN, Lisa et al.The Journal of urology. 2012, Vol 188, Num 4, pp 1613-1617, issn 0022-5347, 5 p., 2Conference Paper

Clues to an Early Diagnosis of Kallmann SyndromeKAPLAN, Julie D; BERNSTEIN, Jonathan A; KWAN, Andrea et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 11, pp 2796-2801, issn 1552-4825, 6 p.Article

A case surviving for over a year of renal tubular dysgenesis with compound heterozygous angiotensinogen gene mutationsUEMATSU, Mitsugu; SAKAMOTO, Osamu; NISHIO, Toshiyuki et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 21, pp 2355-2360, issn 1552-4825, 6 p.Article

Renal functional reserve in children with apparently normal congenital solitary functioning kidneyPECO-ANTIC, Amira; PARIPOVIC, Dusan; KOTUR-STEVULJEVIC, Jelena et al.Clinical biochemistry. 2012, Vol 45, Num 15, pp 1173-1177, issn 0009-9120, 5 p.Article

PAX2 Mutations in Fetal Renal HypodysplasiaMARTINOVIC-BOURIEL, Jelena; BENACHI, Alexandra; ATTIE-BITACH, Tania et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 4, pp 830-835, issn 1552-4825, 6 p.Article

Unilateral renal agenesis and the congenital solitary functioning kidney : developmental, genetic and clinical perspectivesWOOLF, Adrian S; HILLMAN, Katherine A.BJU international (Papier). 2007, Vol 99, Num 1, pp 17-21, issn 1464-4096, 5 p.Article

Didelphic uterus and obstructed hemivagina : Recurrent hematometra in spite of appropriate classic surgical treatmentDONNEZ, Olivier; JADOUL, Pascale; SQUIFFLET, Jean et al.Gynecologic and obstetric investigation. 2007, Vol 63, Num 2, pp 98-101, issn 0378-7346, 4 p.Article

Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios : Role of the renin-angiotensin systemLACOSTE, Mireille; YI CAI; DANIEL, Laurent et al.Journal of the American Society of Nephrology. 2006, Vol 17, Num 8, pp 2253-2263, issn 1046-6673, 11 p.Article

Neonatal Detection of 5p13.2 Duplication and Delineation of the PhenotypeCARRASCOSA ROMERO, M. Carmen; GARCIA HOYO, Rosa; CALVENTE, Maria et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 4, pp 877-881, issn 1552-4825, 5 p.Article

A Case of Maternal Phenylketonuria Syndrome Presenting With Unilateral Renal AgenesisGOKMEN, Tulin; OGUZ, Serife Suna; ALTUG, Nahide et al.Journal of tropical pediatrics (1980). 2011, Vol 57, Num 2, pp 138-140, issn 0142-6338, 3 p.Article

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