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Human Genetics|May 1, 1991
Aldosterone deficiency II (CMO II deficiency) is not the result of a mutation of an MspI restriction site within the CYP11B geneA Mayerovà, B Zieger, M Brandis, et al.
Hormone Research|January 1, 1982
Urinary free T4 and T3 in healthy infants and during noise exposureW von Petrykowski, I Welbers de Liddle, L Kapitel, et al.
Deutsche Medizinische Wochenschrift (1946)|May 18, 1984
[Iodine excretion and dietary iodine supply in newborn infants in iodine-deficient regions of West Germany]P H Heidemann, P Stubbe, K von Reuss, et al.
Helvetica Paediatrica Acta|September 1, 1982
Adrenal insufficiency, myopathic hypotonia, severe psychomotor retardation, failure to thrive, constipation and bladder ectasia in 2 brothers: adrenomyodystrophyW von Petrykowski, R Beckmann, N Böhm, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Sporadic congenital hyperthyroidism due to a spontaneous germline mutation in the thyrotropin receptor geneH P Holzapfel, P Wonerow, W von Petrykowski, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 29, 1998
Autosomal dominant nonautoimmune hyperthyroidism. Clinical features-diagnosis-therapyD Führer, M Mix, H Willgerodt, et al.
The Journal of Pediatrics|December 1, 1990
Adult height in boys and girls with untreated short stature and constitutional delay of growth and puberty: accuracy of five different methods of height predictionJ H Brämswig, M Fasse, M L Holthoff, et al.
Clinical Neuropathology|March 1, 1985
Primary systemic carnitine deficiency under successful therapy: clinical, biochemical, ultrahistochemical and renal clearance studiesW von Petrykowski, U P Ketelsen, E Schmidt-Sommerfield, et al.
Archives of Disease in Childhood|June 1, 1993
Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasia (3A) syndromeD B Grant, N D Barnes, M Dumic, et al.
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