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    1. Moreno, G; Bobadilla, NA; Gonzalez-Salazar, J; Mercado, A; Tapia, E; Hong, E; Herrera-Acosta, J; Gamba, G
      Thiazide-sensitive cotransporter mRMA expression is not altered in three models of hypertension

      KIDNEY & BLOOD PRESSURE RESEARCH
    2. Yu, ASL
      Evolving concepts in epithelial magnesium transport

      CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
    3. Schepkens, H; Stubbe, J; Hoeben, H; Vanholder, R; Lameire, N
      Severe hyponatraemia and hypouricaemia in Gitelman's syndrome

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    4. Tsuchiya, H; Kamoi, K; Soda, S; Sasaki, H; Kobayashi, K; Hayashi, M
      Gitelman's syndrome first diagnosed as Bartter's syndrome

      INTERNAL MEDICINE
    5. Hubner, CA; Stein, V; Hermans-Borgmeyer, I; Meyer, T; Ballanyi, K; Jentsch, TJ
      Disruption of KCC2 reveals an essential role of K-Cl cotransport already in early synaptic inhibition

      NEURON
    6. Ledoussal, C; Lorenz, JN; Nieman, ML; Soleimani, M; Schultheis, PJ; Shull, GE
      Renal salt wasting in mice lacking NHE3 Na+/H+ exchanger but not in mice lacking NHE2

      AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
    7. Schepkens, H; Hoeben, H; Vanholder, R; Lameire, N
      Mimicry of surreptitious diuretic ingestion and the ability to make a genetic diagnosis

      CLINICAL NEPHROLOGY
    8. Hildebrandt, F
      Molecular genetics of renal tubular disorders

      NIEREN-UND HOCHDRUCKKRANKHEITEN
    9. Bonfante, L; Davis, PA; Spinello, M; Antonello, A; D'Angelo, A; Semplicini, A; Calo, L
      Chronic renal failure, end-stage renal disease, and peritoneal dialysis inGitelman's syndrome

      AMERICAN JOURNAL OF KIDNEY DISEASES
    10. Meneton, P; Warnock, DG
      Involvement of renal apical Na transport systems in the control of blood pressure

      AMERICAN JOURNAL OF KIDNEY DISEASES
    11. Urbizu, JM; Gainza, FJ; Lampreabe, I
      Molecular basis of inherited tubular disorders affecting electrolytes and water transport

      NEFROLOGIA
    12. Luft, FC
      Molecular genetics of salt-sensitivity and hypertension

      DRUG METABOLISM AND DISPOSITION
    13. Di Stefano, A; Jounier, S; Wittner, M
      Evidence supporting a role for KCl cotransporter in the thick ascending limb of Henle's loop

      KIDNEY INTERNATIONAL
    14. Calo, L; Ceolotto, G; Milani, M; Pagnin, E; van den Heuvel, LP; Sartori, M; Davis, PA; Costa, R; Semplicini, A
      Abnormalities of Gq-mediated cell signaling in Bartter and Gitelman syndromes

      KIDNEY INTERNATIONAL
    15. Cruz, DN; Shaer, AJ; Bia, MJ; Lifton, RP; Simon, DB
      Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life

      KIDNEY INTERNATIONAL
    16. Arrighi, I; Bloch-Faure, M; Grahammer, F; Bleich, M; Warth, R; Mengual, R; Drici, MD; Barhanin, J; Meneton, P
      Altered potassium balance and aldosterone secretion in a mouse model of human congenital long QT syndrome

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    17. Schmidt, H; Kabesch, M; Schwarz, HP; Kiess, W
      Clinical, biochemical and molecular genetic data in five children with Gitelman's syndrome

      HORMONE AND METABOLIC RESEARCH
    18. Sayer, JA; Pearce, SHS
      Diagnosis and clinical biochemistry of inherited tubulopathies

      ANNALS OF CLINICAL BIOCHEMISTRY
    19. Amirlak, I; Dawson, KP
      Bartter syndrome: an overview

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    20. Gamba, G
      Electroneutral chloride-coupled co-transporters

      CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
    21. Konrad, M; Vollmer, M; Lemmink, HH; Van den Heuvel, LPWJ; Jeck, N; Vargas-Poussou, R; Lakings, A; Ruf, R; Deschenes, G; Antignac, C; Guay-Woodford, L; Knoers, NVAM; Seyberth, HW; Feldmann, D; Hildebrandt, F
      Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    22. Monkawa, T; Kurihara, I; Kobayashi, K; Hayashi, M; Saruta, T
      Novel mutations in thiazide-sensitive Na-Cl cotransporter gene of patientswith Gitelman's syndrome

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    23. Calo, L; Davis, PA; Semplicini, A
      Control of vascular tone in the syndromes of Bartter and Gitelman

      CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES
    24. Friedman, PA
      Mechanisms of renal calcium transport

      EXPERIMENTAL NEPHROLOGY
    25. Thakker, RV
      Molecular pathology of renal chloride channels in Dent's disease and Bartter's syndrome

      EXPERIMENTAL NEPHROLOGY
    26. Weber, S; Hoffmann, K; Jeck, N; Saar, K; Boeswald, M; Kuwertz-Broeking, E; Meij, IIC; Knoers, NVAM; Cochat, P; Sulakova, T; Bonzel, KE; Soergel, M; Manz, F; Schaerer, K; Seyberth, HW; Reis, A; Konrad, M
      Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

      EUROPEAN JOURNAL OF HUMAN GENETICS
    27. Vollmer, M; Jeck, N; Lemmink, HH; Vargas, R; Feldmann, D; Konrad, M; Beekmann, F; van den Heuvel, LPWJ; Deschenes, G; Guay-Woodford, LM; Antignac, C; Seyberth, HW; Hildebrandt, F; Knoers, NVAM
      Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    28. Jeck, N; Konrad, M; Hess, M; Seyberth, HW
      The diuretic- and Bartter-like salt-losing tubulopathies

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    29. Bettinelli, A; Ciarmatori, S; Cesareo, L; Tedeschi, S; Ruffa, G; Appiani, AC; Rosini, A; Grumieri, G; Mercuri, B; Sacco, M; Leozappa, G; Binda, S; Cecconi, M; Navone, C; Curcio, C; Syren, ML; Casari, G
      Phenotypic variability in Bartter syndrome type I

      PEDIATRIC NEPHROLOGY
    30. Uchida, S
      In vivo role of CLC chloride channels in the kidney

      AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
    31. Ellison, DH
      Divalent cation transport by the distal nephron: insights from Bartter's and Gitelman's syndromes

      AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
    32. Rezkalla, L; Borra, S
      Saline-resistant metabolic alkalosis, severe hypokalemia and hypertension in a 74-year-old woman

      CLINICAL NEPHROLOGY
    33. Vezzoli, G; Soldati, L; Jansen, A; Pierro, L
      Choroidal calcifications in patients with Gitelman's syndrome

      AMERICAN JOURNAL OF KIDNEY DISEASES
    34. Calo, L; Punzi, L; Semplicini, A
      Hypomagnesemia and chondrocalcinosis in Bartter's and Gitelman's syndrome:Review of the pathogenetic mechanisms

      AMERICAN JOURNAL OF NEPHROLOGY
    35. Melander, O; Orho-Melander, M; Bengtsson, K; Lindblad, U; Rastam, L; Groop, L; Hulthen, UL
      Genetic variants of thiazide-sensitive NaCl-cotransporter in Gitelman's syndrome and primary hypertension

      HYPERTENSION
    36. Sharma, P; Fatibene, J; Ferraro, F; Jia, HY; Monteith, S; Brown, C; Clayton, D; O'Shaughnessy, K; Brown, MJ
      A genome-wide search for susceptibility loci to human essential hypertension

      HYPERTENSION
    37. Shmukler, BE; Brugnara, C; Alper, SL
      Structure and genetic polymorphism of the mouse KCC1 gene

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    38. Schnermann, J
      NaCl transport deficiencies - hemodynamics to the rescue

      PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
    39. Jeck, N; Konrad, M; Peters, M; Weber, S; Bonzel, KE; Seyberth, HW
      Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype

      PEDIATRIC RESEARCH
    40. Gerelsaikhan, T; Turner, RJ
      Transmembrane topology of the secretory Na+-K+-2Cl(-) cotransporter NKCC1 studied by in vitro translation

      JOURNAL OF BIOLOGICAL CHEMISTRY
    41. Van't Hoff, WG
      Molecular developments in renal tubulopathies

      ARCHIVES OF DISEASE IN CHILDHOOD
    42. Abdel-Al, YK; Badawi, MH; Yaeesh, SAL; Habib, YQ; Al-Khuffash, FA; Al-Ghanim, MM; Al-Najidi, AK
      Bartter's syndrome in Arabic children: review of 13 cases

      PEDIATRICS INTERNATIONAL
    43. Bachmann, S
      Cell localization and ontogeny of sodium transport pathways in the distal nephron: perspectives in function and failure

      CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
    44. Persu, A; Lafontaine, JJ; Devuyst, O
      Chronic hypokalaemia in young women - it is not always abuse of diuretics

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    45. Reimann, R; Gross, D
      Chronic, diagnosis-resistant hypokalaemia

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    46. Su, WF; Shmukler, BE; Chernova, MM; Stuart-Tilley, AK; De Franceschi, L; Brugnara, C; Alper, SL
      Mouse K-Cl cotransporter KCC1: cloning, mapping, pathological expression, and functional regulation

      AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
    47. Kunchaparty, S; Palcso, M; Berkman, J; Velazquez, H; Desir, GV; Bernstein, P; Reilly, RF; Ellison, DH
      Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome

      AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
    48. Meyburg, J; Mayatepek, E; Riester, U; Himbert, U; Zilow, EP; Hilgenfeldt, U; Bremer, HJ; Linderkamp, O
      Clinical symptoms, biochemical studies and therapeutic approaches in a sibship with a new congenital tubulopathy

      EUROPEAN JOURNAL OF PEDIATRICS
    49. Schoof, E; Marx, M; Doerr, HG
      A boy presenting with familial short stature - Diagnosis Gitelman syndrome

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    50. Calo, L; Davis, PA; Milani, M; Cantaro, S; Antonello, A; Favaro, S; D'Angelo, A
      Increased endothelial nitric oxide synthase mRNA level in Bartter's and Gitelman's syndrome - Relationship to vascular reactivity

      CLINICAL NEPHROLOGY
    51. Yahata, K; Tanaka, I; Kotani, M; Mukoyama, M; Ogawa, Y; Goto, M; Nakagawa, M; Sugawara, A; Tanaka, K; Shimatsu, A; Nakao, K
      Identification of a novel R642C mutation in Na/Cl cotransporter with Gitelman's syndrome

      AMERICAN JOURNAL OF KIDNEY DISEASES
    52. Guay-Woodford, LM
      Overview: The genetics of renal disease

      SEMINARS IN NEPHROLOGY
    53. Dell, KM; Guay-Woodford, LM
      Inherited tubular transport disorders

      SEMINARS IN NEPHROLOGY
    54. Vargas-Poussou, R; Forestier, L; Jean, G; Niaudet, P; Dechaux, M; Antignac, C
      Bartter syndrome and Gitelman syndrome.

      ANNALES DE PEDIATRIE
    55. Bhandari, S
      The pathophysiological and molecular basis of Bartter's and Gitelman's syndromes

      POSTGRADUATE MEDICAL JOURNAL
    56. Bettinelli, A; Rusconi, R; Ciarmatori, S; Righini, V; Zammarchi, E; Donati, MA; Isimbaldi, C; Bevilacqua, M; Cesareo, L; Tedeschi, S; Garavaglia, R; Casari, G
      Gitelman disease associated with growth hormone deficiency, disturbances in vasopressin secretion and empty sella: A new hereditary renal tubular-pituitary syndrome?

      PEDIATRIC RESEARCH
    57. Seldin, DW
      Renal handling of calcium

      NEPHRON
    58. Flagg, TP; Tate, M; Merot, J; Welling, PA
      A mutation linked with Bartter's syndrome locks Kir 1.1a (ROMK1) - Channels in a closed state

      JOURNAL OF GENERAL PHYSIOLOGY
    59. Schnermann, J; Briggs, JP
      The macula densa is worth its salt

      JOURNAL OF CLINICAL INVESTIGATION
    60. Mount, DB; Mercado, A; Song, LY; Xu, J; George, AL; Delpire, E; Gamba, G
      Cloning and characterization of KCC3 and KCC4, new members of the cation-chloride cotransporter gene family

      JOURNAL OF BIOLOGICAL CHEMISTRY
    61. Liaw, LCT; Banerjee, K; Coulthard, MG
      Dose related growth response to indometacin(star) in Gitelman syndrome

      ARCHIVES OF DISEASE IN CHILDHOOD
    62. Vantyghem, MC; Douillard, C; Binaut, R; Provot, F
      Bartter's syndromes

      ANNALES D ENDOCRINOLOGIE
    63. Meij, IC; Saar, K; van den Heuvel, LPWJ; Nuernberg, G; Vollmer, M; Hildebrandt, F; Reis, A; Monnens, LAH; Knoers, NVAM
      Hereditary isolated renal magnesium loss maps to chromosome 11q23

      AMERICAN JOURNAL OF HUMAN GENETICS
    64. PEARCE SHS
      STRAIGHTENING OUT THE RENAL TUBULE - ADVANCES IN THE MOLECULAR-BASIS OF THE INHERITED TUBULOPATHIES

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    65. HILDEBRANDT F
      MOLECULAR-GENETICS AND CLINICAL PHENOTYPE IN HERITABLE DISORDERS OF TUBULAR NA+ TRANSPORT

      Kidney & blood pressure research
    66. PUNZI L; CALO L; SCHIAVON F; PIANON M; ROSADA M; TODESCO S
      CHONDROCALCINOSIS IS A FEATURE OF GITELMANS VARIANT OF BARTTERS-SYNDROME - A NEW LOOK AT THE HYPOMAGNESEMIA ASSOCIATED WITH CALCIUM PYROPHOSPHATE DIHYDRATE CRYSTAL DEPOSITION DISEASE

      Revue du rhumatisme
    67. THAKKER RV
      THE ROLE OF RENAL CHLORIDE CHANNEL MUTATIONS IN KIDNEY-STONE DISEASE AND NEPHROCALCINOSIS

      Current opinion in nephrology and hypertension
    68. SIMON DB; LIFTON RP
      ION TRANSPORTER MUTATIONS IN GITELMANS AND BARTTERS SYNDROMES

      Current opinion in nephrology and hypertension
    69. SCHULTHEIS PJ; CLARKE LL; MENETON P; MILLER ML; SOLEIMANI M; GAWENIS LR; RIDDLE TM; DUFFY JJ; DOETSCHMAN T; WANG T; GIEBISCH G; ARONSON PS; LORENZ JN; SHULL GE
      RENAL AND INTESTINAL ABSORPTIVE DEFECTS IN MICE LACKING THE NHE3 NA+ H+ EXCHANGER/

      Nature genetics
    70. ABULADZE N; YANAGAWA N; LEE I; JO OD; NEWMAN D; HWANG J; UYEMURA K; PUSHKIN A; MODLIN RL; KURTZ I
      PERIPHERAL-BLOOD MONONUCLEAR-CELLS EXPRESS MUTATED NCCT MESSENGER-RNAIN GITELMANS-SYNDROME - EVIDENCE FOR ABNORMAL THIAZIDE-SENSITIVE NACLCOTRANSPORT

      Journal of the American Society of Nephrology
    71. NONOGUCHI H; ITOH K; IKEBE M; TOMITA K
      REGULATION OF THE RENAL NA K/2CL COTRANSPORTER GENE - PHYSIOLOGICAL MODULATION IN HEALTH AND ABNORMAL FUNCTION IN DISEASE/

      Experimental nephrology
    72. SIMON DB; LIFTON RP
      MUTATIONS IN NA(K)CL TRANSPORTERS IN GITELMANS AND BARTTERS-SYNDROMES

      Current opinion in cell biology
    73. KAROLYI L; KOCH MC; GRZESCHIK KH; SEYBERTH HW
      THE MOLECULAR-GENETIC APPROACH TO BARTTERS-SYNDROME

      Journal of molecular medicine
    74. MONNENS L; BINDELS R; GRUNFELD JP
      GITELMAN-SYNDROME COMES OF AGE

      Nephrology, dialysis, transplantation
    75. RODRIGUEZSORIANO J
      BARTTER AND RELATED SYNDROMES - THE PUZZLE IS ALMOST SOLVED

      Pediatric nephrology
    76. TURMAN MA
      CONCOMITANT OCCURRENCE OF GITELMAN AND BARTTER SYNDROMES IN THE SAME FAMILY

      Pediatric nephrology
    77. MOOREHOON ML; TURNER RJ
      MOLECULAR CHARACTERIZATION OF THE CATION-CHLORIDE COTRANSPORTER FAMILY

      European journal of morphology
    78. HISAKAWA N; YASUOKA N; ITOH H; TAKAO T; JINNOUCHI C; NISHIYA K; HASHIMOTO K
      A CASE OF GITELMANS-SYNDROME WITH CHONDROCALCINOSIS

      Endocrine journal
    79. HAYASHI M
      SYMPOSIUM ON MORBIDITY OF BODY-FLUID BALANCE AND ITS TREATMENT - 4 - PHYSIOLOGY AND PATHOPHYSIOLOGY OF ACID-BASE HOMEOSTASIS IN THE KIDNEY

      Internal medicine
    80. HOLTZMAN EJ; KUMAR S; FAALAND CA; WARNER F; LOGUE PJ; ERICKSON SJ; RICKEN G; WALDMAN J; KUMAR S; DUNHAM PB
      CLONING, CHARACTERIZATION, AND GENE ORGANIZATION OF K-CL COTRANSPORTER FROM PIG AND HUMAN KIDNEY AND C-ELEGANS

      American journal of physiology. Renal, fluid and electrolyte physiology
    81. HEBERT SC
      ROLES OF NA-K-2CL AND NA-CL COTRANSPORTERS AND ROMK POTASSIUM CHANNELS IN URINARY CONCENTRATING MECHANISM

      American journal of physiology. Renal, fluid and electrolyte physiology
    82. CALO L; DAVIS PA; MILANI M; CANTARO S; BONFANTE L; FAVARO S; DANGELO A
      BARTTERS-SYNDROME AND GITELMANS-SYNDROME - 2 ENTITIES SHARING THE SAME ABNORMALITY OF VASCULAR REACTIVITY

      Clinical nephrology
    83. GREGORY MJ; SCHWARTZ GJ
      DIAGNOSIS AND TREATMENT OF RENAL TUBULAR DISORDERS

      Seminars in nephrology
    84. KELEPOURIS E; AGUS ZS
      HYPOMAGNESEMIA - RENAL MAGNESIUM HANDLING

      Seminars in nephrology
    85. DOMINICZAK AF; JEFFS B; CONNELL JMC
      NEW GENETIC CONCEPTS IN HYPERTENSIVE CARDIOVASCULAR-DISEASE

      Current opinion in cardiology
    86. GASCON A; COBETA JC; IGLESIAS E
      IS GITELMANS-SYNDROME AN ACQUIRED DISEASE

      British journal of rheumatology (Print)
    87. Luft, FC
      Molecular genetics of human hypertension

      JOURNAL OF HYPERTENSION
    88. MORENO G; MERINO A; MERCADO A; HERRERA JP; GONZALEZSALAZAR J; CORREAROTTER R; HEBERT SC; GAMBA G
      ELECTRONEUTRAL NA-COUPLED COTRANSPORTER EXPRESSION IN THE KIDNEY DURING VARIATIONS OF NACL AND WATER METABOLISM

      Hypertension
    89. KURTZ I
      MOLECULAR PATHOGENESIS OF BARTTERS AND GITELMANS SYNDROMES

      Kidney international
    90. LEMMINK HH; KNOERS NVAM; KAROLYI L; VANDIJK H; NIAUDET P; ANTIGNAC C; GUAYWOODFORD LM; GOODYER PR; CAREL JC; HERMES A; SEYBERTH HW; MONNENS LAH; VANDENHEUVEL LPWJ
      NOVEL MUTATIONS IN THE THIAZIDE-SENSITIVE NACL COTRANSPORTER GENE IN PATIENTS WITH GITELMAN-SYNDROME WITH PREDOMINANT LOCALIZATION TO THE C-TERMINAL DOMAIN

      Kidney international
    91. TAKENAKA M; IMAI E; KANEKO T; ITO T; MORIYAMA T; YAMAUCHI A; HORI M; KAWAMOTO S; OKUBO K
      ISOLATION OF GENES IDENTIFIED IN MOUSE RENAL PROXIMAL TUBULE BY COMPARING DIFFERENT GENE-EXPRESSION PROFILES

      Kidney international
    92. FRIEDMAN PA
      CODEPENDENCE OF RENAL CALCIUM AND SODIUM-TRANSPORT

      Annual review of physiology
    93. Gamba, G; Moreno, G
      The role of renal interstitial pressure on the chronic control of arterialblood pressure

      REVISTA DE INVESTIGACION CLINICA
    94. LHOTTA K; GRUBER J; SGONC R; FEND F; KONIG P
      APOPTOSIS OF TUBULAR EPITHELIAL-CELLS IN FAMILIAL JUVENILE GOUTY NEPHROPATHY

      Nephron
    95. Bhandari, S; Turney, JH
      The molecular basis of hypokalaemic alkalosis: Bartter's and Gitelman's syndromes

      NEPHRON
    96. MOUNT DB; DELPIRE E; GAMBA G; HALL AE; POCH E; HOOVER RS; HEBERT SC
      THE ELECTRONEUTRAL CATION-CHLORIDE COTRANSPORTERS

      Journal of Experimental Biology
    97. SCHULTHEIS PJ; LORENZ JN; MENETON P; NIEMAN ML; RIDDLE TM; FLAGELLA M; DUFFY JJ; DOETSCHMAN T; MILLER ML; SHULL GE
      PHENOTYPE RESEMBLING GITELMANS-SYNDROME IN MICE LACKING THE APICAL NA-CL- COTRANSPORTER OF THE DISTAL CONVOLUTED TUBULE()

      The Journal of biological chemistry
    98. GUAYWOODFORD LM
      BARTTER-SYNDROME - UNRAVELING THE PATHOPHYSIOLOGIC ENIGMA

      The American journal of medicine
    99. SIMON DB; BINDRA RS; MANSFIELD TA; NELSONWILLIAMS C; MENDONCA E; STONE R; SCHURMAN S; NAYIR A; ALPAY H; BAKKALOGLU A; RODRIGUEZSORIANO J; MORALES JM; SANJAD SA; TAYLOR CM; PILZ D; BREM A; TRACHTMAN H; GRISWOLD W; RICHARD GA; JOHN E; LIFTON RP
      MUTATIONS IN THE CHLORIDE CHANNEL GENE, CLCNKB, CAUSE BARTTERS-SYNDROME TYPE-III

      Nature genetics
    100. WALDER RY; SHALEV H; BRENNAN TMH; CARMI R; ELBEDOUR K; SCOTT DA; HANAUER A; MARK AL; PATIL S; STONE EM; SHEFFIELD VC
      FAMILIAL HYPOMAGNESEMIA MAPS TO CHROMOSOME 9Q, NOT TO THE X-CHROMOSOME - GENETIC-LINKAGE MAPPING AND ANALYSIS OF A BALANCED TRANSLOCATION BREAKPOINT

      Human molecular genetics


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Documento generato il 07/06/20 alle ore 06:09:23