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	1.	Chromosome 5q subtelomeric deletion syndrome. [electronic resource] by Rauch, Anita Dörr, Helmuth-Günther Producer: 20080117 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 145C Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Circadian rhythm of salivary cortisol, 17alpha-hydroxyprogesterone, and progesterone in healthy children. [electronic resource] by Gröschl, Michael Rauh, Manfred Dörr, Helmuth-Günther Producer: 20031107 In: Clinical chemistry vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Maternal administration of high dose vitamin D3 for cerebral palsy in her child. [electronic resource] by Zimmermann, Bettina Dörr, Helmuth-Günther Müller, Wolfgang Dötsch, Jörg Producer: 20040831 In: European journal of pediatrics vol. 163 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Diagnosis of endocrine disease: limitations of the IGF1 generation test in children with short stature. [electronic resource] by Coutant, Régis Dörr, Helmuth-Günther Gleeson, Helena Argente, Jesús Producer: 20120420 In: European journal of endocrinology vol. 166 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	GENETICS IN ENDOCRINOLOGY: Gain and loss of function mutations of the calcium-sensing receptor and associated proteins: current treatment concepts. [electronic resource] by Mayr, Bernhard Schnabel, Dirk Dörr, Helmuth-Günther Schöfl, Christof Producer: 20160809 In: European journal of endocrinology vol. 174 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Iodine deficiency and subclinical hypothyroidism are common in cystic fibrosis patients. [electronic resource] by Naehrlich, Lutz Dörr, Helmuth-Günther Bagheri-Behrouzi, Azadeh Rauh, Manfred Producer: 20130904 In: Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Variable White Matter Atrophy and Intellectual Development in a Family With X-linked Creatine Transporter Deficiency Despite Genotypic Homogeneity. [electronic resource] by Heussinger, Nicole Saake, Marc Mennecke, Angelika Dörr, Helmuth-Günther Trollmann, Regina Producer: 20171218 In: Pediatric neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Pediatric renal allograft transplantation does not normalize the increased cortisol/cortisone ratios of chronic renal failure. [electronic resource] by Schroth, Michael Plank, Christian Rauh, Manfred Dörr, Helmuth-Günther Rascher, Wolfgang Dötsch, Jörg Producer: 20060526 In: European journal of endocrinology vol. 154 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Intellectual outcome, motor skills and BMI of children with congenital hypothyroidism: a population-based study. [electronic resource] by Arenz, Stephan Nennstiel-Ratzel, Uta Wildner, Manfred Dörr, Helmuth-Günther von Kries, Rüdiger Producer: 20080812 In: Acta paediatrica (Oslo, Norway : 1992) vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Psychometric properties of the quality of life in short statured youth (QoLISSY) questionnaire within the course of growth hormone treatment. [electronic resource] by Bloemeke, Janika Silva, Neuza Bullinger, Monika Witt, Stefanie Dörr, Helmuth-Günther Quitmann, Julia Producer: 20190508 In: Health and quality of life outcomes vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Children with classic congenital adrenal hyperplasia experience salt loss and hypoglycemia: evaluation of adrenal crises during the first 6 years of life. [electronic resource] by Odenwald, Brigitte Nennstiel-Ratzel, Uta Dörr, Helmuth-Günther Schmidt, Heinrich Wildner, Manfred Bonfig, Walter Producer: 20160506 In: European journal of endocrinology vol. 174 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Two cases of thyroid dysgenesis caused by different novel PAX8 mutations in the DNA-binding region: in vitro studies reveal different pathogenic mechanisms. [electronic resource] by Hermanns, Pia Grasberger, Helmut Cohen, Ronald Freiberg, Clemens Dörr, Helmuth-Günther Refetoff, Samuel Pohlenz, Joachim Producer: 20140127 In: Thyroid : official journal of the American Thyroid Association vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Hypoparathyroidism in conotruncal heart defects. [electronic resource] by Koch, Andreas Hofbeck, Michael Buheitel, Gernot Dörr, Helmuth-Günther Rauch, Anita Rauch, Ralf Singer, Helmut Producer: 20030204 In: European journal of pediatrics vol. 161 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Cortisol-cortisone ratios in small for gestational age (SGA) children without postnatal catch-up growth. [electronic resource] by Plank, Christian Meissner, Udo Rauh, Manfred Wollmann, Hartmut Dörr, Helmuth-Günther Rascher, Wolfgang Dötsch, Jörg Producer: 20080110 In: Clinical endocrinology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Diffuse Encephalopathy Associated with Isolated Cerebral Langerhans Cell Histiocytosis. [electronic resource] by Rompel, Oliver Buslei, Rolf Hammon, Matthias Dörr, Helmuth-Günther Chada, Martin Nikkhah, Guido Uder, Michael Trollmann, Regina Producer: 20171218 In: Pediatric neurology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Familial short stature due to a 5q22.1-q23.2 duplication refines the 5q duplication spectrum. [electronic resource] by Zahnleiter, Diana Trautmann, Udo Ekici, Arif B Goehring, Ina Reis, André Dörr, Helmuth-Günther Rauch, Anita Thiel, Christian T Producer: 20111206 In: European journal of medical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	First report of ectopic ACTH syndrome and PTHrP-induced hypercalcemia due to a hepatoblastoma in a child. [electronic resource] by Grunewald, Thomas G P von Luettichau, Irene Welsch, Ulrich Dörr, Helmuth-Günther Höpner, Frank Kovacs, Kalman Burdach, Stefan Rabl, Wolfgang Producer: 20100427 In: European journal of endocrinology vol. 162 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Central laboratory reassessment of IGF-I, IGF-binding protein-3, and GH serum concentrations measured at local treatment centers in growth-impaired children: implications for the agreement between outpatient screening and the results of somatotropic axis functional testing. [electronic resource] by Hauffa, Berthold P Lehmann, Nils Bettendorf, Markus Mehls, Otto Dörr, Helmuth-Günther Stahnke, Nikolaus Steinkamp, Heinz Said, Elfriede Ranke, Michael B Producer: 20071206 In: European journal of endocrinology vol. 157 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Two novel mutations in the insulin binding subunit of the insulin receptor gene without insulin binding impairment in a patient with Rabson-Mendenhall syndrome. [electronic resource] by Thiel, Christian T Knebel, Birgit Knerr, Ina Sticht, Heinrich Müller-Wieland, D Zenker, Martin Reis, Andre Dörr, Helmuth-Günther Rauch, Anita Producer: 20080915 In: Molecular genetics and metabolism vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	A de novo 7.6Mb tandem duplication of 14q32.2-qter associated with primordial short stature with neurosecretory growth hormone dysfunction, distinct facial anomalies and mild developmental delay. [electronic resource] by Thiel, Christian T Dörr, Helmuth-Günther Trautmann, Udo Hoyer, Juliane Hofmann, Kristin Kraus, Cornelia Ekici, Arif B Reis, André Rauch, Anita Producer: 20081014 In: European journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 30 results.