P. Heidemann

发表

Extracorporeal photochemotherapy as an effective treatment modality in chronic graft-versus-host disease

B. Balda, A. Konstantinow, H. Starz, 1996 .

Chronic graft‐versus‐host disease: successful treatment with extracorporeal photochemotherapy: a follow‐up

B. Balda, A. Konstantinow, H. Starz, 1996, The British journal of dermatology.

Noonan syndrome: growth and clinical manifestations in 144 cases

M. Ranke, A. Schmaltz, P. Heidemann, 1988, European Journal of Pediatrics.

Five novel mutations in steroidogenic factor 1 (SF1, NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency

A. Grüters, H. Biebermann, B. Köhler, 2008, Human mutation.

Congenital Disorder of Glycosylation IId (CDG-IId) - A New Entity: Clinical Presentation with Dandy-Walker Malformation and Myopathy

G. Hoffmann, V. Peters, C. Körner, 2002, Neuropediatrics.

A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I

T. Meitinger, C. Scharfe, T. Klopstock, 2000, Journal of medical genetics.

Aggregate formation of erythrocytes and diabetic retinopathy in children, adolescents, and adults with diabetes mellitus (type I)

M. Lakomek, P. Heidemann, W. Behrens-Baumann, 1984, Klinische Wochenschrift.

Characterization of eleven novel mutations (M45L, R119H, 544delG, G145V, H154Y, C184Y, D289V, 862+5A, 1172delC, R411X, E459K) in the tissue‐nonspecific alkaline phosphatase (TNSALP) gene in patients with severe hypophosphatasia

R. Brenner, F. Muller, O. Boute, 1999 .

Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity.

W. Friedrich, C. Doglioni, E. Gambineri, 2008, The Journal of allergy and clinical immunology.

Wide phenotypic variability in families with holoprosencephaly and a sonic hedgehog mutation

P. Heidemann, U. Hehr, A. Hehr, 2004, European Journal of Pediatrics.

Activating mutations in the calcium‐sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia – a German survey

M. Wabitsch, H. Dörr, C. Schöfl, 2011, Clinical endocrinology.

Clinical and Functional Characterization of a Patient Carrying a Compound Heterozygous Pericentrin Mutation and a Heterozygous IGF1 Receptor Mutation

D. Friebe, W. Kiess, J. Kratzsch, 2012, PloS one.

Hypergonadotropic hypogonadism, SHBG deficiency and hyperprolactinaemia: A transient phenomenon during induction chemotherapy in leukemic children

S. Schwarz, P. Heidemann, P. Stubbe, 1982, European Journal of Pediatrics.

Multiple endokrine Neoplasie Typ 2 (MEN 2) im Kindes- und Jugendalter

H. Dralle, P. Heidemann, R. Tratzmüller, 1999, Monatsschrift Kinderheilkunde.

Iodine-induced alterations of thyroid function in newborn infants after prenatal and perinatal exposure to povidone iodine.

A. Grüters, D. L'Allemand, P. Heidemann, 1983, The Journal of pediatrics.

Gonadoblastoma Y locus genes expressed in germ cells of individuals with dysgenetic gonads and a Y chromosome in their karyotypes include DDX3Y and TSPY

P. Sinn, P. Vogt, T. Strowitzki, 2019, Human reproduction.

Complete virilization in congenital adrenal hyperplasia: clinical course, medical management and disease‐related complications

H. Wollmann, N. Albers, J. Brämswig, 2002, Clinical endocrinology.

Transient secondary hypothyroidism and thyroxine binding globulin deficiency in leukemic children during polychemotherapy: An effect of L-asparaginase

P. Heidemann, P. Stubbe, W. Beck, 1981, European Journal of Pediatrics.

Disseminated choriocarcinoma in infancy is curable by chemotherapy and delayed tumour resection.

P. Ambros, D. V. von Schweinitz, D. Harms, 2001, European journal of cancer.

Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.

E. Berger, K. von Figura, C. Thiel, 2002, The Journal of clinical investigation.

Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)

S. Schnittger, F. Beermann, I. Hansmann, 1989, Human Genetics.

Insulin Tolerance Test Causes Hypokalaemia and Can Provoke Cardiac Arrhythmias

G. Binder, M. Ranke, P. Heidemann, 2004, Hormone Research in Paediatrics.

Regional variations of iodine nutrition and thyroid function during the neonatal period in Europe.

R. Vigneri, C. Beckers, F. Delange, 1986, Biology of the neonate.

A familial progressive neurodegenerative disease with 2-oxoglutaric aciduria

U. Langenbeck, G. Hoffmann, P. Heidemann, 1982, European Journal of Pediatrics.

Serum 3,5,3'-triiodothyronine, thyroxine, and thyrotropin in hypothyroid infants with congenital goiter and the response to iodine.

P. Heidemann, P. Stubbe, 1978, The Journal of clinical endocrinology and metabolism.

Functioning thoracic paraganglioma: association with Von Hippel-Lindau syndrome.

H. Neumann, A. Januszewicz, R. Gärtner, 1997, The Journal of clinical endocrinology and metabolism.

Characteristics, management modalities and outcome in chronic systolic heart failure patients treated in tertiary care centers: results from the EVIdence based TreAtment in Heart Failure (EVITA-HF) registry

J. Brachmann, M. Böhm, M. Hochadel, 2014, Clinical Research in Cardiology.

Transient congenital hypothyroidism after amniofetography

P. Heidemann, P. Schürnbrand, P. Stubbe, 1980, European Journal of Pediatrics.

Incidence of iodine contamination in neonatal transient hyperthyrotropinemia

A. Grüters, D. L'Allemand, P. Heidemann, 1983, European Journal of Pediatrics.

Phaeochromocytoma associated with a de novo VHL mutation as form fruste of von Hippel-Lindau disease

K. Zerres, H. Neumann, H. Dörr, 2001, European Journal of Pediatrics.

Effect of different oestrogen doses on final height reduction in girls with constitutional tall stature

A. Grüters, P. Heidemann, H. Helge, 1989, European Journal of Pediatrics.

Characterization of eleven novel mutations (M45L, R119H, 544delG, G145V, H154Y, C184Y, D289V, 862+5A, 1172delC, R411X, E459K) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in patients with severe hypophosphatasia. Mutations in brief no. 217. Online.

R. Brenner, F. Muller, O. Boute, 1999, Human mutation.

Influence of iodine prophylaxis on thyroid function and iodine excretion in newborn infants and their mothers: comparison between Sweden and Germany

P. Heidemann, P. Stubbe, N. Skanke, 1986 .

Thyroxine-Binding Globulin, Triiodothyronine, Thyroxine and Thyrotropin in Newborn Infants and Children

R. Hesch, P. Heidemann, P. Stubbe, 1978, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Iodine deficiency and brain development.

P. Heidemann, P. Stubbe, F. Schulte, 1986, Bibliotheca nutritio et dieta.

Iodine-induced hypothyroidism and goiter following lipiodolTM lymphography

G. Prindull, P. Heidemann, P. Schürnbrand, 1982, European Journal of Pediatrics.

Bi-allelic inactivation of the MEN1 tumor suppressor gene in human grade II astrocytoma.

B. Karges, W. Karges, L. Ludwig, 2003, Cancer letters.