H. Frisch

发表

Pulsatile secretion of gonadotropins in early infancy

F. Waldhauser, A. Pollak, G. Weißenbacher, 1981, European Journal of Pediatrics.

Growth hormone replacement therapy is not associated with retinal changes.

M. Clodi, A. Luger, M. Riedl, 2000, The Journal of clinical endocrinology and metabolism.

Hyperprolactinemia, a Tool in Treatment Control of Tetrahydrobiopterin Deficiency: Endocrine Studies in an Affected Girl

F. Waldhauser, N. Blau, C. Bieglmayer, 1998, Pediatric Research.

Differential effects of growth hormone therapy in malnourished hemodialysis patients.

W. Hörl, G. Mayer, A. Luger, 2001, Kidney international.

Response of gonadotropins to stimulation with luteinizing hormone -- releasing hormone (LH-RH) in children with precocious puberty before, during and following therapy with cyproterone acetate or an ethisterone derivate.

H. Frisch, P. Kemeter, I. Steinert, 1977, Padiatrie und Padologie. Supplementum.

Beta-cell function recovery is not the only factor responsible for remission in type I diabetics: evaluation of C-peptide secretion in diabetic children after first metabolic recompensation and at partial remission phase

G. Schernthaner, E. Schober, H. Frisch, 1984, Journal of endocrinological investigation.

FALL IN NOCTURNAL SERUM MELATONIN DURING PREPUBERTY AND PUBESCENCE

R. Wurtman, F. Waldhauser, H. Frisch, 1984, The Lancet.

Volume Regulation and Renal Function at High Altitude across Gender

N. Goswami, A. Roessler, H. Hinghofer-Szalkay, 2015, PloS one.

Effects of 12 months of recombinant growth hormone therapy on parameters of bone metabolism and bone mineral density in patients on chronic hemodialysis.

F. Kainberger, W. Hörl, G. Mayer, 2004, Journal of nephrology.

One-Year Growth Hormone Therapy Improves Granulocyte Function without Major Effects on Nutritional and Anthropometric Parameters in Malnourished Hemodialysis Patients

W. Hörl, G. Mayer, A. Luger, 2003, Nephron Clinical Practice.

Perspectives of longitudinal growth in cystic fibrosis from birth to adult age

T. Waldhör, G. Haeusler, M. Götz, 1994, European Journal of Pediatrics.

Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia.

T. Battelino, F. Waldhauser, S. Baumgartner-Parzer, 2005, European journal of endocrinology.

Diminished prolactin response to thyrotropin and insulin in anorexia nervosa.

F. Waldhauser, J. Spona, H. Frisch, 1984, The Journal of clinical endocrinology and metabolism.

Effect of growth hormone treatment on hormonal parameters, body composition and strength in athletes.

W. Blum, T. Waldhör, H. Frisch, 1993, Acta endocrinologica.

Growth hormone and body composition in athletes.

H. Frisch, 1999, Journal of endocrinological investigation.

Incidence of Childhood Diabetes Mellitus in Austria 1979–1984

E. Schober, H. Frisch, 1988, Acta paediatrica Scandinavica.

Fluorescence angiography of the paramacular retinal vessels and altered glomerular basement membrane in children with juvenile onset diabetes mellitus

G. Simbruner, G. Lubec, E. Schober, 2007, Acta diabetologia latina.

A pilot study of growth hormone therapy in dilated cardiomyopathy

R. Birnbacher, M. Marx, H. Frisch, 1999, European Journal of Pediatrics.

Methods for evaluation of growth in Turner's syndrome: critical approach and review of the literature

G. Haeusler, H. Frisch, 1994, Acta paediatrica.

Spontaneous Growth in Growth Hormone Deficiency from Birth until 7 Years of Age: Development of Disease-Specific Growth Curves

K. Kapelari, H. Frisch, M. Voigt, 2010, Hormone Research in Paediatrics.

Apolipoproteins and Lipoproteins in Children with Type I Diabetes: Relation to Glycosylated Serum Protein and HbA1

K. Widhalm, E. Schober, A. Pollak, 1985, Acta paediatrica Scandinavica.

Clinical aspects of insulin-like growth factor binding proteins.

L. Giudice, Y. Hasegawa, R. Rosenfeld, 1991, Acta endocrinologica.

Increase of Serum Lipids and Serum Lipoproteins in Girls under Therapy with Estrogen and Norethisteron for Height Reduction

K. Widhalm, E. Schober, M. Weninger, 1987, Acta paediatrica Scandinavica.

Effects of Growth Hormone (GH) and Insulin-like Growth Factor-I Therapy in patients with Gene Defects in the GH Axis

S. Riedl, H. Frisch, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Procedure for Neonatal Screening for Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

M. Knip, G. Schackert, A. Ruokonen, 2001, Hormone Research in Paediatrics.

Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia.

T. Battelino, F. Waldhauser, S. Baumgartner-Parzer, 2005, European journal of endocrinology.

Adaptation of ghrelin and the GH/IGF axis to high altitude.

T. Waldhör, M. Kluge, S. Riedl, 2012, European journal of endocrinology.

Evidence for genetic control of anti-insulin immunity in juvenile onset diabetes mellitus.

W. Mayr, G. Schernthaner, H. Frisch, 1977, Diabete & metabolisme.

Self-administration of cadaveric growth hormone in power athletes

H. Frisch, R. Deyssig, 1993, The Lancet.

SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity.

G. Binder, M. Ranke, V. Hesse, 2004, The Journal of clinical endocrinology and metabolism.

Validation of a Mathematical Model Predicting the Response to Growth Hormone Treatment in Prepubertal Children with Idiopathic Growth Hormone Deficiency

J. Lebl, S. Riedl, T. Zidek, 2004, Hormone Research in Paediatrics.

Primary growth hormone (GH) insensitivity and insulin-like growth factor deficiency caused by novel compound heterozygous mutations of the GH receptor gene: genetic and functional studies of simple and compound heterozygous states.

B. Little, V. Hwa, S. Amselem, 2007, The Journal of clinical endocrinology and metabolism.

Total absence of functional acid labile subunit, resulting in severe insulin-like growth factor deficiency and moderate growth failure.

B. Little, V. Hwa, R. Rosenfeld, 2006, The Journal of clinical endocrinology and metabolism.

Growth hormone therapy with three dosage regimens in children with idiopathic short stature

J. Wit, J. Chaussain, G. Massa, 1998 .

Growth hormone therapy with three dosage regimens in children with idiopathic short stature. European Study Group Participating Investigators.

H. Delemarre-van de Waal, J. Wit, P. Chatelain, 1998, The Journal of pediatrics.

Spontaneous growth in idiopathic short stature. European Study Group.

J. Wit, M. Ranke, J. Chaussain, 1996, Archives of disease in childhood.

Bayley-Pinneau, Roche-Wainer-Thissen, and Tanner height predictions in normal children and in patients with various pathologic conditions.

A. Prader, M. Zachmann, B. Sobradillo, 1978, The Journal of pediatrics.

SCREENING FOR CONGENITAL HYPOTHYROIDISM

H. Frisch, M. Weissel, H. Fritzsche, 1976, The Lancet.

Waardenburg syndrome type 2 in a Turkish family: implications for the importance of the pattern of fundus pigmentation

A. Read, H. Frisch, E. Moser, 2001, The British journal of ophthalmology.

Aldosterone and testosterone producing adrenal adenoma in childhood

E. Schober, H. Frisch, N. Neuhold, 1995, Journal of endocrinological investigation.

Combined pituitary hormone deficiency and pituitary hypoplasia due to a mutation of the Pit‐1 gene

R. Pfäffle, H. Frisch, G. Häusler, 2000, Clinical endocrinology.

Treatment of patients with Ullrich-Turner syndrome with conventional doses of growth hormone and the combination with testosterone or oxandrolone: Effect on growth, IGF-I and IGFBP-3 concentrations

T. Waldhör, G. Haeusler, M. Zachmann, 1995, European Journal of Pediatrics.

The influence of growth hormone monotherapy and growth hormone in combination with oxandrolone or testosterone on thyroxid hormone parameters and thyrxine binding globulin in patients with Ullrich- Turner syndrome

T. Waldhör, H. Frisch, G. Häusler, 1997, European Journal of Pediatrics.

Influence of estrogen administration on growth hormone response to GHRH and L-Dopa in patients with Turner's syndrome.

F. Waldhauser, E. Schober, H. Frisch, 1989, Acta endocrinologica.

P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia.

W. Miller, J. Phillips, H. Frisch, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Growth data in large series of 587 children and adolescents with type 1 diabetes mellitus.

E. Schober, M. Šnajderová, S. Pruhova, 2003, Endocrine regulations.

Julv 1983 / 3 cell function in siblings of diabetic children and HLA type

W. Mayr, G. Schernthaner, E. Schober, 2006 .

Beta cell function in siblings of diabetic children and HLA type.

W. Mayr, G. Schernthaner, E. Schober, 1983, Archives of disease in childhood.

Treatment of growth failure with growth hormone in children with chronic kidney disease: an open-label long-term study.

T. Tulassay, Z. Zadik, L. Bell, 2010, Clinical nephrology.

Raymond's syndrome following petrosal sinus sampling

J. Honegger, W. Huk, R. Fahlbusch, 2005, Acta Neurochirurgica.

Growth hormone in combination with anabolic steroids in patients with Turner syndrome: effect on bone maturation and final height.

T. Waldhör, G. Haeusler, H. Frisch, 1996, Acta paediatrica.

Longitudinal growth in HIV-negative boys with haemophilia

V. Komrska, C. Male, J. Lebl, 2000, European Journal of Pediatrics.

Effect of growth hormone treatment on glucose tolerance in a patient with cystinosis after kidney transplantation.

E. Schober, C. Kohlhauser, H. Frisch, 1995, Klinische Padiatrie.

Alterations in nocturnal serum melatonin levels in humans with growth and aging.

M. Schemper, F. Waldhauser, H. Frisch, 1988, The Journal of clinical endocrinology and metabolism.

Screening of patients with Turner syndrome for "hidden" Y-mosaicism.

G. Kronberger, O. Rittinger, G. Fekete, 1999, Klinische Padiatrie.

Congenital Adrenal Hyperplasia: Lessons from a Multinational Study

T. Battelino, F. Waldhauser, J. Sólyom, 2002, Hormone Research in Paediatrics.

Lessons from 30 years of clinical diagnosis and treatment of congenital adrenal hyperplasia in five middle European countries.

G. Heinze, T. Battelino, F. Waldhauser, 2001, The Journal of clinical endocrinology and metabolism.

Hormonal, genetic and clinical findings in an XX male.

R. Birnbacher, H. Frisch, 1995, Hormone research.

Gender Identity Reversal in an Adolescent with Mixed Gonadal Dysgenesis

R. Birnbacher, E. Schober, G. Weißenbacher, 1999, Journal of pediatric endocrinology & metabolism : JPEM.

Serum melatonin is not affected by glucocorticoid replacement in congenital adrenal hyperplasia.

F. Waldhauser, C. Bieglmayer, E. Schober, 1986, Acta endocrinologica.

Growth after radiotherapy and chemotherapy in children with leukemia or lymphoma.

H. Frisch, E. Schuster, L. Thun-Hohenstein, 1992, Hormone research.

Neurofibromatosis 1: A Novel NF1 Mutation in an 11-Year-Old Girl With a Giant Cell Granuloma

M. Rasse, K. Wimmer, H. Frisch, 2003, Journal of child neurology.

Mutational spectrum of the steroid 21-hydroxylase gene in Austria: identification of a novel missense mutation.

F. Waldhauser, W. Waldhäusl, S. Baumgartner-Parzer, 2001, The Journal of clinical endocrinology and metabolism.

Pronounced short stature in a girl with tricho‐rhino‐phalangeal syndrome II (TRPS II, Langer–Giedion syndrome) and growth hormone deficiency

F. Grill, H. Lüdecke, S. Riedl, 2004, American journal of medical genetics. Part A.

Salt Wasting in Simple Virilizing Congenital Adrenal Hyperplasia

S. Baumgartner-Parzer, P. Nowotny, H. Vierhapper, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

Capillary gas chromatography as a tool for characterization of urinary steroid excretion in patients with congenital adrenal hyperplasia.

W. Waldhäusl, P. Nowotny, H. Vierhapper, 1985, Journal of steroid biochemistry.

Familial Combined Pituitary Hormone Deficiency Caused by PROP-1 Gene Mutation

D. Prayer, H. Stobbe, R. Pfäffle, 2002, Hormone Research in Paediatrics.

Mutations in PROP1 cause familial combined pituitary hormone deficiency

John A. Phillips, Joy D. Cogan, Wei Wu, 1998, Nature Genetics.

GONADOTROPIN RESPONSIVENESS TO LUTEINIZING HORMONE RELEASING HORMONE IN PREPUBERTAL AND PUBERTAL PATIENTS WITH GROWTH HORMONE DEFICIENCY

L. Havelec, F. Waldhauser, G. Schernthaner, 1982, Acta paediatrica Scandinavica.

Constitutional chromosome anomalies in patients with cerebral gigantism (Sotos syndrome).

O. Haas, E. Schober, G. Haeusler, 1993, Klinische Padiatrie.

Death in two female Prader-Willi syndrome patients during the early phase of growth hormone treatment.

S. Riedl, H. Frisch, P. Blümel, 2005, Acta paediatrica.

[Neonatal screening for congenital hypothyroidism].

H. Frisch, W. Strobl, D. Möslinger, 1997, Acta medica Austriaca.

LEUKAEMIA AND GROWTH HORMONE

H. Frisch, E. Balzar, L. Thun-Hohenstein, 1988, The Lancet.

Death in two female Prader‐Willi syndrome patients during the early phase of growth hormone treatment

S. Riedl, H. Frisch, P. Blümel, 2005 .

RITODRINE AND SERUM MELATONIN LEVELS

F. Waldhauser, H. Frisch, E. Tatzer, 1983, The Lancet.

Psychological Aspects in Children and Adolescents with Hypopituitarism

H. Frisch, G. Häusler, S. Singer, 1990 .

Mutations and Pituitary Morphology in a Series of 82 Patients with PROP1 Gene Defects

W. Blum, O. Cinek, R. Verkauskienė, 2011, Hormone Research in Paediatrics.

Refining clinical phenotypes in septo-optic dysplasia based on MRI findings

D. Prayer, P. Brugger, T. Battelino, 2008, European Journal of Pediatrics.

Lymphocyte subsets in renal transplant recipients during growth hormone therapy.

A. Šedivá, H. Krásnicanová, J. Lebl, 1999, Endocrine regulations.

Prolactin and thyrotrophin response to thyrotrophin-releasing hormone in growth hormone deficiency.

F. Waldhauser, E. Schober, K. Herkner, 1982, Archives of disease in childhood.

Diagnosis of Growth Hormone Excess and Hyperprolactinemia

S. Riedl, H. Frisch, 2011 .

Long-Term Treatment in Children with Hypopituitarism: Pubertal Development and Final Height

R. Birnbacher, S. Riedl, H. Frisch, 1998, Hormone Research in Paediatrics.

Septo‐optic dysplasia and growth hormone deficiency: accelerated pubertal maturation during GH therapy

D. Wimberger, F. Waldhauser, F. Aichner, 1992, Acta paediatrica.

Defects of Growth Hormone Genes

J. Phillips, Á. Ferrández, K. Zuppinger, 1986 .

Short- and long-term (final height) data in children with normal variant short stature treated with growth hormone

T. Waldhör, H. Frisch, P. Blümel, 1997, European Journal of Pediatrics.

Growth hormone (GH) treatment to final height in children with idiopathic short stature: evidence for a dose effect.

Brenda J. Crowe, J. Wit, J. Chaussain, 2005, The Journal of pediatrics.

Circadian patterns of plasma cortisol, 17-hydroxyprogesterone, and testosterone in congenital adrenal hyperplasia.

E. Schober, H. Frisch, W. Swoboda, 1981, Archives of disease in childhood.

Congenital hypothyroidism in a Turkish family: the role of immunoglobulins blocking the trophic effects of TSH and maternal-foetal relationship.

H. Drexhage, G. Wick, R. van der Gaag, 1986, Acta endocrinologica.

Familial Athyreotic Cretinism

E. Schober, M. Weissel, H. Frisch, 1981, Pediatric Research.

Auxological, Ophthalmological, Neurological and MRI Findings in 25 Austrian Patients with Septo-Optic Dysplasia (SOD)

D. Prayer, G. Bernert, S. Riedl, 2002, Hormone Research in Paediatrics.

FINAL HEIGHT IN 22 PATIENTS WITH IDIOPATHIC GROWTH HORMONE (GH) DEFICIENCY AFTER LONG TERM TREATMENT WITH GH

F. Waldhauser, E. Schober, H. Frisch, 1986, Pediatric Research.

Pituitary hyperplasia in a girl with gonadal dysgenesis and primary hypothyroidism.

S. Riedl, H. Frisch, 1997, Hormone research.

Growth Patterns and Final Height in Congenital Adrenal Hyperplasia due to Classical 21-Hydroxylase Deficiency

T. Battelino, F. Waldhauser, R. Hauspie, 2001, Hormone Research in Paediatrics.

Diagnosis of X-recessive Kallmann syndrome in early infancy

R. Birnbacher, H. Frisch, K. Wandl-Vergesslich, 1994, European Journal of Pediatrics.

Short- and long-term (final height) growth responses to growth hormone (GH) therapy in patients with Turner syndrome: correlation of growth response to stimulated GH levels, spontaneous GH secretion, and karyotype.

G. Haeusler, H. Frisch, P. Blümel, 1997, Hormone research.

Insulin, insulin-like growth factor-binding protein-1, and sex hormone-binding globulin in patients with Turner's syndrome: course over age in untreated patients and effect of therapy with growth hormone alone and in combination with oxandrolone.

T. Waldhör, G. Haeusler, H. Frisch, 1996, The Journal of clinical endocrinology and metabolism.

Growth retardation and reduced growth hormone secretion in a boy with achalasia

E. Schober, H. Frisch, 1995, European Journal of Pediatrics.

The effect of substance L on glucose-mediated cross-links of collagen in the diabetic db/db mouse.

G. Lubec, R. Mallinger, H. Höger, 1990, Nephron.

GLYCOSYLATED HEMOGLOBIN (HbAtc) AND PLASMA LIPOPROTEINS IN JUVENILE ONSET DIABETES MELLITUS

L. Havelec, K. Widhalm, E. Schober, 1980, Acta paediatrica Scandinavica.

18p monosomy with GH‐deficiency and empty sella: good response to GH‐treatment

E. Schober, H. Frisch, S. Scheibenreiter, 1995, Clinical genetics.

[Ring chromosome 15 in a child (author's transl)].

H. Frisch, S. Scheibenreiter, 1978, Wiener klinische Wochenschrift.

Abstracts: 18th ANNUAL MEETING

F. Waldhauser, J. Spona, H. Frisch, 1979, Pediatric Research.

HLA-DR ANTIGENS AND THYROID AUTOANTIBODIES IN DIABETIC CHILDREN

W. Mayr, E. Schober, H. Frisch, 1984, Pediatric Research.

MELATONIN SECRETION IN TURNER'S SYNDROME: LACK OF EFFECT OF OESTROGEN ADMINISTRATION

F. Waldhauser, C. Bieglmayer, E. Schober, 1989, Clinical endocrinology.

Spontaneous 24-h ghrelin secretion pattern in fasting subjects: maintenance of a meal-related pattern.

S. Riedl, T. Zidek, H. Frisch, 2005, European journal of endocrinology.

Effects of insulin-like growth factor I on basal and stimulated glucose fluxes in rat liver.

M. Roden, W. Waldhäusl, H. Frisch, 2000, The Biochemical journal.

GROWTH HORMONE BLOCKING ANTIBODIES IN A PATIENT WITH DELETION OF THE GH‐N GENE

R. Moncayo, S. Schwarz, J. Phillips, 1987, Clinical endocrinology.

Growth hormone treatment in Turner's syndrome: short and long‐term effects on metabolic parameters

G. Haeusler, H. Frisch, Herwig Frisch, 1992, Clinical endocrinology.

Spontaneous growth in turner syndrome: Evidence for a minor pubertal growth spurt

M. Schemper, G. Haeusler, H. Frisch, 1992, European Journal of Pediatrics.

GH and TSH deficiency [letter]

B. Otten, R. Pfäffle, J. Lebl, 1998 .

[Reduction of body height in tall girls by estrogen treatment].

F. Waldhauser, E. Schober, M. Weninger, 1992, Klinische Padiatrie.

Final height and pubertal development in children with growth hormone deficiency after long-term treatment.

R. Birnbacher, H. Frisch, 1995, Hormone Research.

Increase in 6-hydroxymelatonin excretion in humans during ascent to high altitudes.

F. Waldhauser, T. Waldhör, P. Neupane, 2004, The Journal of clinical endocrinology and metabolism.

A pharmacological dose of melatonin increases PRL levels in males without altering those of GH, LH, FSH, TSH, testosterone or cortisol.

M. Schemper, H. Lieberman, R. Wurtman, 1987, Neuroendocrinology.

Hypoplasia of the corpus callosum and growth hormone deficiency in the XXXXY syndrome.

A. Neuhold, G. Haeusler, F. Hadžiselimović, 1992, American journal of medical genetics.

DÉPARTEMENT MÉDICO-CHIRURGICAL DE PÉDIATRIE CHEF DE DÉPARTEMENT Professeur Sergio Fanconi SPONTANEOUS 24h GHRELIN SECRETION PATTERN IN FASTING SUBJECTS : MAINTENANCE OF A MEAL-RELATED PATTERN

S. Riedl, T. Zidek, H. Frisch, 2014 .

Adaptation of ghrelin and the GH/IGF axis to high altitude.

T. Waldhör, M. Kluge, S. Riedl, 2012, European journal of endocrinology.

Computer-aided estimation of skeletal age and comparison with bone age evaluations by the method of Greulich-Pyle and Tanner-Whitehouse

T. Waldhör, S. Riedl, H. Frisch, 2005, Pediatric Radiology.

Heterogeneous growth hormone (GH) gene mutations in familial GH deficiency.

J. Cogan, E. Schober, J. Phillips, 1993, The Journal of clinical endocrinology and metabolism.