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Human Leptin Deficiency Caused by a Missense Mutation: Multiple Endocrine Defects, Decreased Sympathetic Tone, and Immune System Dysfunction Indicate New Targets for Leptin Action, Greater Central than Peripheral Resistance to the Effects of Leptin, and Spontaneous Correction of Leptin-Mediated Defects

The journal of clinical endocrinology and metabolism, 1999-10, Vol.84 (10), p.3686-3695

1999

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Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

American journal of human genetics, 2008-10, Vol.83 (4), p.511-519

2008

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Bektashi Baba Dr. Hasan Ragip Erensel: One of Ataturk's Doctors/ ATATURK'UN DOKTORLARINDAN BEKTASI BABASI DR. HASAN RAGIP ERENSEL/ Einer der Arzte Ataturks: Der bektaschitische Baba Dr. Hasan Ragip Erensel

Journal of Alevism-Bektashism Studies, 2024-06, Vol.29, p.197

Ozata, Metin

2024

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Phenotypic effects of leptin replacement on morbid obesity, diabetes mellitus, hypogonadism, and behavior in leptin-deficient adults

Proceedings of the National Academy of Sciences - PNAS, 2004-03, Vol.101 (13), p.4531-4536

2004

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Effect of Leptin Replacement on Brain Structure in Genetically Leptin-Deficient Adults

The journal of clinical endocrinology and metabolism, 2005-05, Vol.90 (5), p.2851-2854

2005

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Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome

Fertility and sterility, 2011-04, Vol.95 (5), p.1613-1620.e7

2011

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Increased oxidative stress and hypozincemia in male obesity

Clinical biochemistry, 2002-11, Vol.35 (8), p.627-631

2002

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Synchronicity of Frequently Sampled Thyrotropin (TSH) and Leptin Concentrations in Healthy Adults and Leptin-Deficient Subjects: Evidence for Possible Partial TSH Regulation by Leptin in Humans

The journal of clinical endocrinology and metabolism, 2001-07, Vol.86 (7), p.3284-3291

2001

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The Effects of Metformin and Diet on Plasma Testosterone and Leptin Levels in Obese Men

Obesity (Silver Spring, Md.), 2001-11, Vol.9 (11), p.662-667

2001

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Atatürk’ün Doktorlarından Bektaşi Babası Dr. Hasan Ragıp Erensel

ALEVİLİK–BEKTAŞİLİK ARAŞTIRMALARI DERGİSİ, 2024-06 (29), p.197-210

Özata, Metin

2024

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Molecular Scanning for Mutations in the Insulin Receptor Substrate-1 (Irs-1) Gene in Turkish with Type 2 Diabetes Mellitus

Endocrine Journal, 2005, Vol.52(5), pp.593-598

2005

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WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

American journal of human genetics, 2010-10, Vol.87 (4), p.465-479

2010

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TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

The journal of clinical endocrinology and metabolism, 2010-06, Vol.95 (6), p.2857-2867

2010

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Oxidative stress and nitric oxide related parameters in type II diabetes mellitus: effects of glycemic control

Clinical biochemistry, 2001-02, Vol.34 (1), p.65-70

2001

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A leptin missense mutation associated with hypogonadism and morbid obesity

Nature genetics, 1998-03, Vol.18 (3), p.213-215

1998

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Low serum leptin level in colon cancer patients without significant weight loss

Tumori, 2002-03, Vol.88 (2), p.147-149

2002

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Different Presentation of Bone Mass in Mice and Humans with Congenital Leptin Deficiency

The journal of clinical endocrinology and metabolism, 2002-02, Vol.87 (2), p.951-951

Ozata, Metin

2002

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Molecular Scanning for Mutations in the Insulin Receptor Substrate-1 (Irs-1) Gene in Turkish with Type 2 Diabetes Mellitus

ENDOCRINE JOURNAL, 2005, Vol.52 (5), p.593-598

2005

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Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism

Fertility and sterility, 2006-03, Vol.85 (3), p.706-713

2006

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GnRH-Deficient Phenotypes in Humans and Mice with Heterozygous Variants in KISS1/Kiss1

The journal of clinical endocrinology and metabolism, 2011-11, Vol.96 (11), p.E1771-E1781

2011

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A novel melanocortin 4 receptor (MC4R) gene mutation associated with morbid obesity

The journal of clinical endocrinology and metabolism, 2001-07, Vol.86 (7), p.3448-3451

2001

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Comparison of Electrocardiographic Repolarization Patterns between Hypogonad Males and Normal Subjects

Annals of noninvasive electrocardiology, 2003-10, Vol.8 (4), p.284-288

2003

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The effect of subclinical hypothyroidism on platelet parameters

Hematology (Luxembourg), 2009-04, Vol.14 (2), p.115-117

2009

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Synchronicity of frequently sampled thyrotropin (TSH) and leptin concentrations in healthy adults and leptin-deficient subjects : Evidence for possible partial TSH regulation by leptin in humans

The journal of clinical endocrinology and metabolism, 2001-07, Vol.86 (7), p.3284-3291

2001

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Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Bektashi Baba Dr. Hasan Ragip Erensel: One of Ataturk's Doctors/ ATATURK'UN DOKTORLARINDAN BEKTASI BABASI DR. HASAN RAGIP ERENSEL/ Einer der Arzte Ataturks: Der bektaschitische Baba Dr. Hasan Ragip Erensel

Phenotypic effects of leptin replacement on morbid obesity, diabetes mellitus, hypogonadism, and behavior in leptin-deficient adults

Effect of Leptin Replacement on Brain Structure in Genetically Leptin-Deficient Adults

Heterozygous mutations in SOX2 may cause idiopathic hypogonadotropic hypogonadism via dominant-negative mechanisms

Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome

Increased oxidative stress and hypozincemia in male obesity

Synchronicity of Frequently Sampled Thyrotropin (TSH) and Leptin Concentrations in Healthy Adults and Leptin-Deficient Subjects: Evidence for Possible Partial TSH Regulation by Leptin in Humans

The Effects of Metformin and Diet on Plasma Testosterone and Leptin Levels in Obese Men

Atatürk’ün Doktorlarından Bektaşi Babası Dr. Hasan Ragıp Erensel

Molecular Scanning for Mutations in the Insulin Receptor Substrate-1 (Irs-1) Gene in Turkish with Type 2 Diabetes Mellitus

WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

Oxidative stress and nitric oxide related parameters in type II diabetes mellitus: effects of glycemic control

A leptin missense mutation associated with hypogonadism and morbid obesity

Low serum leptin level in colon cancer patients without significant weight loss

Different Presentation of Bone Mass in Mice and Humans with Congenital Leptin Deficiency

Molecular Scanning for Mutations in the Insulin Receptor Substrate-1 (Irs-1) Gene in Turkish with Type 2 Diabetes Mellitus

Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism

GnRH-Deficient Phenotypes in Humans and Mice with Heterozygous Variants in KISS1/Kiss1

A novel melanocortin 4 receptor (MC4R) gene mutation associated with morbid obesity

Comparison of Electrocardiographic Repolarization Patterns between Hypogonad Males and Normal Subjects

The effect of subclinical hypothyroidism on platelet parameters

Synchronicity of frequently sampled thyrotropin (TSH) and leptin concentrations in healthy adults and leptin-deficient subjects : Evidence for possible partial TSH regulation by leptin in humans

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