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Association of HLA alleles and haplotypes with CYP21A2 gene p. V282L mutation in the Croatian population

HLA, 2016-11, Vol.88 (5), p.239-244

2016

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Low bone mineral density for age/osteoporosis in triple A syndrome—an overlooked symptom of unexplained etiology

Osteoporosis international, 2016-02, Vol.27 (2), p.521-526

2016

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Characteristics of the craniofacial complex in Turner syndrome

Archives of oral biology, 2010-01, Vol.55 (1), p.81-88

2010

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Alicyclic beta-amino acids in Medicinal Chemistry

Amino acids, 2005-08, Vol.29 (2), p.89-100

2005

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Bone mineral density in children and young adults with Type 1 diabetes mellitus

Bone (New York, N.Y.), 2009-06, Vol.44, p.S287-S287

2009

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4″- O-(ω-Quinolylamino-alkylamino)propionyl derivatives of selected macrolides with the activity against the key erythromycin resistant respiratory pathogens

Bioorganic & medicinal chemistry, 2010-09, Vol.18 (17), p.6559-6568

2010

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Pregnancy outcomes in women with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Journal of Pediatric Endocrinology and Metabolism, 2005-01, Vol.18 (9), p.887

2005

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Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasia (3A) syndrome

Archives of disease in childhood, 1993-06, Vol.68 (6), p.779-782

1993

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Long Term Follow-Up of Clinical and Electromyoneurographical Abnormalities in Eight Croatian Patients with Triple A Syndrome (P01.126)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.P01-P01.126

2012

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Nonclassic 21-hydroxylase deficiency in Croatia

Journal of Pediatric Endocrinology and Metabolism, 2004-02, Vol.17 (2), p.157

2004

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Thyroid diseases in a school population with thyromegaly

Archives of disease in childhood, 1994-02, Vol.70 (2), p.103-106

1994

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O46 – 1548 Long term follow-up of clinical and neurographical abnormalities in eight Croatian patients with triple A syndrome

European journal of paediatric neurology, 2013-09, Vol.17, p.S15-S15

2013

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Xerostomia in patients with triple A syndrome : a newly recognised finding

European journal of pediatrics, 2000-12, Vol.159 (12), p.885-888

2000

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Eur J Pediatr.: Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy

Croatian medical journal, 2011-04, Vol.52 (2), p.224

2011

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Hormones and handedness: left-hand bias in female congenital adrenal hyperplasia patients

Neurology, 1987-04, Vol.37 (4), p.711-711

1987

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Alicyclic [beta]-amino acids in Medicinal Chemistry

Amino acids, 2005-08, Vol.29 (2), p.89

2005

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Apolipoprotein E phenotypes and genotypes as determined by polymerase chain reaction using allele-specific oligonucleotide probes and the amplification refractory mutation system in children with insulin-dependent diabetes mellitus

Clinica chimica acta, 1993-07, Vol.216 (1), p.191-198

1993

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Antihyperglycemic N-sulfonyl-1a,2,6,6a-tetrahydro-1H,4H- [1,3]dioxepino[5,6-b]azirines: synthesis, X-ray structure analysis, conformational behavior, quantitative structure-property relationships, and quantitative structure-activity relationships

Journal of medicinal chemistry, 1995-08, Vol.38 (16), p.3034-3042

1995

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Synthesis, characterization and in vitro antimicrobial activity of novel sulfonylureas of 15-membered azalides

Journal of antibiotics, 2005-06, Vol.58 (6), p.380-389

2005

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Bilateral gonadoblastoma in a 9-month-old infant with 46,XY gonadal dysgenesis

Journal of endocrinological investigation, 1993-04, Vol.16 (4), p.291-293

1993

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Adrenocorticotropic hormone insensitivity associated with autonomic nervous system disorders

European journal of pediatrics, 1991-08, Vol.150 (10), p.696-699

1991

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Interferences with determination of 17-hydroxyprogesterone in amniotic fluid

Clinical chemistry (Baltimore, Md.), 1991-12, Vol.37 (12), p.2154-2155

1991

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A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele

Molecular endocrinology (Baltimore, Md.), 1991-05, Vol.5 (5), p.685-692

1991

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Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) Without Demonstrable Genetic Mutations

The journal of clinical endocrinology and metabolism, 1999-01, Vol.84 (1), p.378-381

1999

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Association of HLA alleles and haplotypes with CYP21A2 gene p. V282L mutation in the Croatian population

Low bone mineral density for age/osteoporosis in triple A syndrome—an overlooked symptom of unexplained etiology

Characteristics of the craniofacial complex in Turner syndrome

Alicyclic beta-amino acids in Medicinal Chemistry

Bone mineral density in children and young adults with Type 1 diabetes mellitus

4″- O-(ω-Quinolylamino-alkylamino)propionyl derivatives of selected macrolides with the activity against the key erythromycin resistant respiratory pathogens

Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)

Pregnancy outcomes in women with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasia (3A) syndrome

Long Term Follow-Up of Clinical and Electromyoneurographical Abnormalities in Eight Croatian Patients with Triple A Syndrome (P01.126)

Nonclassic 21-hydroxylase deficiency in Croatia

Thyroid diseases in a school population with thyromegaly

O46 – 1548 Long term follow-up of clinical and neurographical abnormalities in eight Croatian patients with triple A syndrome

Xerostomia in patients with triple A syndrome : a newly recognised finding

Eur J Pediatr.: Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy

Hormones and handedness: left-hand bias in female congenital adrenal hyperplasia patients

Alicyclic [beta]-amino acids in Medicinal Chemistry

Apolipoprotein E phenotypes and genotypes as determined by polymerase chain reaction using allele-specific oligonucleotide probes and the amplification refractory mutation system in children with insulin-dependent diabetes mellitus

Antihyperglycemic N-sulfonyl-1a,2,6,6a-tetrahydro-1H,4H- [1,3]dioxepino[5,6-b]azirines: synthesis, X-ray structure analysis, conformational behavior, quantitative structure-property relationships, and quantitative structure-activity relationships

Synthesis, characterization and in vitro antimicrobial activity of novel sulfonylureas of 15-membered azalides

Bilateral gonadoblastoma in a 9-month-old infant with 46,XY gonadal dysgenesis

Adrenocorticotropic hormone insensitivity associated with autonomic nervous system disorders

Interferences with determination of 17-hydroxyprogesterone in amniotic fluid

A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele

Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) Without Demonstrable Genetic Mutations

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