H. Toka

发表

Mutations in Kelch-like 3 and Cullin 3 cause hypertension and electrolyte abnormalities

Jai Radhakrishnan, Murim Choi, Robert Bjornson, 2012, Nature.

Severely Impaired Baroreflex-Buffering in Patients With Monogenic Hypertension and Neurovascular Contact

R. Naraghi, A. Diedrich, J. Tank, 2000, Circulation.

Wnk4 controls blood pressure and potassium homeostasis via regulation of mass and activity of the distal convoluted tubule

R. Lifton, C. Nelson-Williams, R. Flavell, 2006, Nature Genetics.

Genetic Syndromes of Renal Hypertension

H. Toka, Hakan R Toka, 2016 .

Could Postmortem Iss and Niss Points Sign Preventable Deaths

H. Toka, K. Karbeyaz, Tarık Gündüz, 2010 .

WNK kinases: molecular regulators of integrated epithelial ion transport.

R. Lifton, K. Kahle, F. H. Wilson, 2004, Current opinion in nephrology and hypertension.

Monogenic forms of human hypertension.

F. Luft, H. Toka, 2002, Seminars in nephrology.

E. Brown, B. Lanske, Xuedong Zhou, 2018, Proceedings of the National Academy of Sciences.

Pregnancy-associated polyuria in familial renal glycosuria.

C. Zera, J. Duffield, D. Mount, 2013, American journal of kidney diseases : the official journal of the National Kidney Foundation.

New functional aspects of the extracellular calcium-sensing receptor

H. Toka, Hakan R Toka, 2014, Current opinion in nephrology and hypertension.

The role of the calcium-sensing receptor in disorders of abnormal calcium handling and cardiovascular disease

H. Toka, M. Pollak, Hakan R Toka, 2014, Current opinion in nephrology and hypertension.

Families with Autosomal Dominant Brachydactyly Type E, Short Stature, and Severe Hypertension

T. Wienker, D. Chitayat, F. Luft, 1998, Annals of Internal Medicine.

Inversion Region for Hypertension and Brachydactyly on Chromosome 12p Features Multiple Splicing and Noncoding RNA

D. Chitayat, F. Luft, Y. Neuenfeld, 2008, Hypertension.

Autosomal-Dominant Hypertension With Type E Brachydactyly Is Caused by Rearrangement on the Short Arm of Chromosome 12

W. Haefeli, A. Busjahn, M. Gollasch, 2004, Hypertension.

Mendelian hypertension with brachydactyly as a molecular genetic lesson in regulatory physiology.

J. Jordan, F. Luft, H. Toka, 2003, American journal of physiology. Regulatory, integrative and comparative physiology.

Heterogeneity of autonomic regulation in hypertension and neurovascular contact

Arya M. Sharma, J. Tank, J. Jordan, 2002, Journal of hypertension.

Absence of hypertensive retinopathy in a Turkish kindred with autosomal dominant hypertension and brachydactyly

F. Luft, H. Toka, L. Hattenbach, 1998, The British journal of ophthalmology.

Multisite measurement of regional oxygen saturation in Fontan patients with and without protein-losing enteropathy at rest and during exercise

M. Rauh, F. Fahlbusch, H. Toka, 2019, Pediatric Research.

Parathyroid hormone controls paracellular Ca2+ transport in the thick ascending limb by regulating the tight-junction protein Claudin14

J. Hou, B. Lanske, N. Ide, 2017, Proceedings of the National Academy of Sciences.

Comparative expression of the extracellular calcium-sensing receptor in the mouse, rat, and human kidney.

D. Riccardi, H. Toka, M. Schepelmann, 2016, American journal of physiology. Renal physiology.

Deficiency of the calcium-sensing receptor in the kidney causes parathyroid hormone-independent hypocalciuria.

E. Brown, G. Curhan, S. Quinn, 2012, Journal of the American Society of Nephrology : JASN.

Lactobacillus acidophilus Endocarditis Complicated by Pauci-Immune Necrotizing Glomerulonephritis

H. Toka, Vivian O. Chukwurah, Comfort Takang, 2020, Case reports in medicine.

Genetic disorders of sodium transport

H. Toka, 2019, Nephrology Secrets.

Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12

T. Wienker, J. Ott, Dennis A Gilbert, 1996, Nature Genetics.

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Andreas Busjahn, Jens Jordan, Herbert Schulz, 2015, Nature Genetics.

Calcium Sensing in the Renal Tubule.

P. Houillier, H. Toka, M. Pollak, 2015, Physiology.

Is the Kidney a Calcium-Sensing Organ ?

P. Houillier, H. Toka, M. Pollak, 2015 .

Clinical Effects of Phosphodiesterase 3A Mutations in Inherited Hypertension With Brachydactyly

J. Schulz-Menger, W. Utz, J. Tank, 2015, Hypertension.

Mitochondrial DNA mutations in renal disease: an overview

D. Bockenhauer, S. Walsh, H. Toka, 2020, Pediatric Nephrology.

Monogenic Forms of Hypertension

H. Toka, Hakan R Toka, 2018 .

Frequency of Rare Allelic Variation in Candidate Genes among Individuals with Low and High Urinary Calcium Excretion

G. Curhan, G. Genovese, D. Mount, 2013, PloS one.

The molecular basis of blood pressure variation

H. Toka, Hakan R Toka, A. Hariri, 2013, Pediatric Nephrology.

Childhood Hypertension in Autosomal-Dominant Hypertension With Brachydactyly

N. Hübner, F. Luft, F. Rüschendorf, 2010, Hypertension.

Mutations in PAX2 associate with adult-onset FSGS.

G. Genovese, V. Caputo, M. Tartaglia, 2014, Journal of the American Society of Nephrology : JASN.

A Cluster of Metabolic Defects Caused by Mutation in a Mitochondrial tRNA

Hongyu Zhao, K. Petersen, G. Shulman, 2004, Science.

Transcriptional Patterns in Peritoneal Tissue of Encapsulating Peritoneal Sclerosis, a Complication of Chronic Peritoneal Dialysis

N. Braun, M. Bhasin, S. Alper, 2013, PloS one.

Congenital anomalies of kidney and urinary tract.

Hiep T Nguyen, H. Toka, O. Toka, 2010, Seminars in nephrology.

Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertension.

T. Wienker, A. Busjahn, F. Luft, 1996, Hypertension.