UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 215

Sortiert nach

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Characteristics of the craniofacial complex in Turner syndrome

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

2010

Volltextzugriff (PDF)

Alicyclic beta-amino acids in Medicinal Chemistry

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

2005

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Journal of pediatric endocrinology & metabolism : JPEM, 2005-01, Vol.18 (9), p.887

2005

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Nonclassic 21-hydroxylase deficiency in Croatia

Journal of pediatric endocrinology & metabolism : JPEM, 2004-02, Vol.17 (2), p.157

2004

Volltextzugriff (PDF)

Thyroid diseases in a school population with thyromegaly

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

1994

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

2000

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

1987

Volltextzugriff (PDF)

Alicyclic [beta]-amino acids in Medicinal Chemistry

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

2005

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Adrenocorticotropic hormone insensitivity associated with autonomic nervous system disorders

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

1991

Volltextzugriff (PDF)

Interferences with determination of 17-hydroxyprogesterone in amniotic fluid

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

1991

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Successful Treatment of Diffuse Large B-Cell Non-Hodgkin Lymphoma with Modified CHOP (Cyclophosphamide/Doxorubicin/Vincristine/ Prednisone) Chemotherapy and Rituximab in a Patient with Nijmegen Syndrome

Clinical lymphoma & myeloma, 2007-11, Vol.7 (9), p.590-593

2007

Volltextzugriff (PDF)

1 – 25 von 215

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(144)
Mit Volltextzugriff
(150)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(149)
Croatian
(62)
Japanisch
(7)
Deutsch
(4)
Serbian
(2)

Erscheinungsjahr

n.n

Thema

Humans
(88)
Science & Technology
(81)
Female
(65)
Life Sciences & Biomedicine
(60)
Male
(47)
Biological And Medical Sciences
(27)
Child
(27)
Medical Sciences
(25)
Adult
(19)
Adolescent
(17)
Infant
(17)
Endocrinology & Metabolism
(16)
Child, Preschool
(14)
Adrenal Hyperplasia, Congenital - Genetics
(13)
Pediatrics
(13)
Chemistry
(12)
Physical Sciences
(12)
Animals
(11)
Endocrinopathies
(11)
Technology
(11)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

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

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

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

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

Successful Treatment of Diffuse Large B-Cell Non-Hodgkin Lymphoma with Modified CHOP (Cyclophosphamide/Doxorubicin/Vincristine/ Prednisone) Chemotherapy and Rituximab in a Patient with Nijmegen Syndrome

Suchergebnisse filtern