N Bilginturan

Hacettepe University

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Co-Authors

Herbert Schuster

Max Delbrück Center

Friedrich C. Luft

Max Delbrück Center

Hakan R. Toka

Max Delbrück Center

Sylvia Bähring

Max Delbrück Center

Okan Toka

Klinikum Fürth

Andreas Busjahn

Charité - Universitätsmedizin Berlin

Hermann Haller

Medizinische Hochschule Hannover

Thomas F. Wienker

Max Planck Institute for Molecular Genetics

Tahsin Teziç

Güven Hospital

ÖÖ

Özgür Öztekin

Izmir University

Cooperative Institutions

Charité - Universitätsmedizin Berlin

Max Delbrück Center

Hacettepe University

Medizinische Hochschule Hannover

Humboldt-Universität zu Berlin

Boston Children's Hospital

Hacettepe University Hospital

Freie Universität Berlin

German Centre for Cardiovascular Research

Harvard University

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

Nature Genetics (1996)

Herbert Schuster Thomas F. Wienker Sylvia Bähring N Bilginturan Hakan R. Toka

Brachydactyly

10.1038/ng0596-98

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Citations (144)

Leprechaunism in two Turkish patients.

PubMed (1997)

Aytemiz Gürgey S Göğüş U Saatçi N Bilginturan N Yordam

We report two cases of Leprechaunism with the classical features. The first case had hyperglycemia and severe hyperinsulinemia. The postmortem examination of the second child revealed enlargement of both ovaries, islet cell hyperplasia in the pancreas, and cholestasis and paucity of bile ducts in the liver. Cystic changes were noted in the ovaries, and the kidneys contained a few small cortical cysts. Both patients died at early ages.

Nesidioblastosis

Hyperinsulinemia

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Citations (4)

Maternal hyperparathyroidism and neonatal rickets

The Journal of Pediatrics (1989)

Şînasi Özsoylu N Bilginturan

10.1016/s0022-3476(89)80591-8

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Citations (2)

Symptomatic hypocalcemia and hypomagnesemia due to gentamicin therapy in an 8-year-old girl.

PubMed (1982)

Tahsin Teziç Y Saraçlar N Bilginturan I Kilcioğlu

Girl

Hypoparathyroidism

Source

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Citations (10)

Dermatoglyphics in patients with a syndrome of brachydactyly, short stature and hypertension.

PubMed (1973)

Kutay Taysi M Atasu Burhan Say N Bilginturan

Brachydactyly

Dermatoglyphics

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Citations (0)

The results of sodium fluoride treatment in osteogenesis imperfecta.

PubMed (1966)

N Bilginturan S Ozsoylu

Sodium fluoride

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Citations (5)

Primary hyperaldosteronism due to bilateral adrenal hyperplasia in a 13 year-old boy.

PubMed (1980)

Tahsin Teziç N Bilginturan M Cağlar N. Gürses

Hyperaldosteronism

Primary (astronomy)

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Citations (0)

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Nature Genetics (2015)

Philipp G. Maass Atakan Aydın Friedrich C. Luft Carolin Schächterle Anja Weise

Brachydactyly

10.1038/ng.3302

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Citations (157)

Hereditary Brachydactyly Associated with Hypertension

Journal of Medical Genetics (1973)

N Bilginturan S Zileli S Karacadağ T. Pırnar

A family showing brachydactyly associated with hypertension is reported. The number and location of the involved bones are quite different from the other cases with brachydactyly reported in the literature. Additionally, all our patients have high blood pressure. We believe that the disorder reported here represents a hitherto undescribed entity. It is thought that both hypertension and brachydactyly are transmitted as an autosomal dominant trait by a single pleiotropic gene or by two closely located genes.

Brachydactyly

10.1136/jmg.10.3.253

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Citations (90)

Responses of children with parathyroid disorders to calcium gluconate (CaGl) and parathormone (Lilly)

The Journal of Pediatrics (1965)

John F. Crigler N Bilginturan

10.1016/s0022-3476(65)81916-3

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Citations (0)