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	241.	Effect of long-term bromocriptine infusion on plasma prolactin and ovine chorionic somatomammotropin in the pregnant ewe and fetal sheep. [electronic resource] by Lowe, K C Beck, N F McNaughton, D C Gluckman, P D Kaplan, S L Grumbach, M M Nathanielsz, P W Producer: 19791229 In: American journal of obstetrics and gynecology vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	242.	Pharmacological evidence for stimulation of growth hormone secretion by a central noradrenergic system in dogs. [electronic resource] by Lovinger, R Holland, J Kaplan, S Grumbach, M Boryczka, A T Shackelford, R Salmon, J Reid, I A Ganong, W F Producer: 20010712 In: Neuroscience vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	243.	Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene. [electronic resource] by Proukakis, C Auer-Grumbach, M Wagner, K Wilkinson, P A Reid, E Patton, M A Warner, T T Crosby, A H Producer: 20030326 In: Human mutation vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	244.	Diabetic neuropathy increases stimulation threshold during popliteal sciatic nerve block. [electronic resource] by Heschl, S Hallmann, B Zilke, T Gemes, G Schoerghuber, M Auer-Grumbach, M Quehenberger, F Lirk, P Hogan, Q Rigaud, M Producer: 20160722 In: British journal of anaesthesia vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	245.	Idiopathic hypothalamic diabetes insipidus, pituitary stalk thickening, and the occult intracranial germinoma in children and adolescents. [electronic resource] by Mootha, S L Barkovich, A J Grumbach, M M Edwards, M S Gitelman, S E Kaplan, S L Conte, F A Producer: 19970523 In: The Journal of clinical endocrinology and metabolism vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	246.	Treatment of true precocious puberty with a potent luteinizing hormone-releasing factor agonist: effect on growth, sexual maturation, pelvic sonography, and the hypothalamic-pituitary-gonadal axis. [electronic resource] by Styne, D M Harris, D A Egli, C A Conte, F A Kaplan, S L Rivier, J Vale, W Grumbach, M M Producer: 19850723 In: The Journal of clinical endocrinology and metabolism vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	247.	Ontogeny and regulation of corticosteroid binding globulin capacity in plasma of fetal and newborn lambs. [electronic resource] by Ballard, P L Kitterman, J A Bland, R D Clyman, R I Gluckman, P D Platzker, A C Kaplan, S L Grumbach, M M Producer: 19820412 In: Endocrinology vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	248.	Role of MRI in the evaluation of ambiguous genitalia. [electronic resource] by Secaf, E Hricak, H Gooding, C A Ho, V W Gorczyca, D P Ringertz, H Conte, F A Kogan, B A Grumbach, M M Producer: 19950126 In: Pediatric radiology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	249.	Long-term outcome in children and adolescents after transsphenoidal surgery for Cushing's disease. [electronic resource] by Devoe, D J Miller, W L Conte, F A Kaplan, S L Grumbach, M M Rosenthal, S M Wilson, C B Gitelman, S E Producer: 19971117 In: The Journal of clinical endocrinology and metabolism vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	250.	SPG10 is a rare cause of spastic paraplegia in European families. [electronic resource] by Schüle, R Kremer, B P H Kassubek, J Auer-Grumbach, M Kostic, V Klopstock, T Klimpe, S Otto, S Boesch, S van de Warrenburg, B P Schöls, L Producer: 20080429 In: Journal of neurology, neurosurgery, and psychiatry vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	251.	Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder? [electronic resource] by De Jonghe, P Auer-Grumbach, M Irobi, J Wagner, K Plecko, B Kennerson, M Zhu, D De Vriendt, E Van Gerwen, V Nicholson, G Hartung, H-P Timmerman, V Producer: 20020724 In: Brain : a journal of neurology vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	252.	Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II. [electronic resource] by Coen, K Pareyson, D Auer-Grumbach, M Buyse, G Goemans, N Claeys, K G Verpoorten, N Laurà, M Scaioli, V Salmhofer, W Pieber, T R Nelis, E De Jonghe, P Timmerman, V Producer: 20060424 In: Neurology vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	253.	Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndrome. [electronic resource] by Auer-Grumbach, M Fischer, C Papić, L John, E Plecko, B Bittner, R E Bernert, G Pieber, T R Miltenberger, G Schwarz, R Windpassinger, C Grill, F Timmerman, V Speicher, M R Janecke, A R Producer: 20080731 In: Neuropediatrics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	254.	High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia. [electronic resource] by Beetz, C Nygren, A O H Schickel, J Auer-Grumbach, M Bürk, K Heide, G Kassubek, J Klimpe, S Klopstock, T Kreuz, F Otto, S Schüle, R Schöls, L Sperfeld, A-D Witte, O W Deufel, T Producer: 20070108 In: Neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	255.	Molecular genetics and pathophysiology of 17 beta-hydroxysteroid dehydrogenase 3 deficiency. [electronic resource] by Andersson, S Geissler, W M Wu, L Davis, D L Grumbach, M M New, M I Schwarz, H P Blethen, S L Mendonca, B B Bloise, W Witchel, S F Cutler, G B Griffin, J E Wilson, J D Russel, D W Producer: 19960220 In: The Journal of clinical endocrinology and metabolism vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	256.	Dominant GDAP1 mutations cause predominantly mild CMT phenotypes. [electronic resource] by Zimoń, M Baets, J Fabrizi, G M Jaakkola, E Kabzińska, D Pilch, J Schindler, A B Cornblath, D R Fischbeck, K H Auer-Grumbach, M Guelly, C Huber, N De Vriendt, E Timmerman, V Suter, U Hausmanowa-Petrusewicz, I Niemann, A Kochański, A De Jonghe, P Jordanova, A Producer: 20110930 In: Neurology vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	257.	SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum. [electronic resource] by Goizet, C Boukhris, A Maltete, D Guyant-Maréchal, L Truchetto, J Mundwiller, E Hanein, S Jonveaux, P Roelens, F Loureiro, J Godet, E Forlani, S Melki, J Auer-Grumbach, M Fernandez, J C Martin-Hardy, P Sibon, I Sole, G Orignac, I Mhiri, C Coutinho, P Durr, A Brice, A Stevanin, G Producer: 20091030 In: Neurology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	258.	Multi-system neurological disease is common in patients with OPA1 mutations. [electronic resource] by Yu-Wai-Man, P Griffiths, P G Gorman, G S Lourenco, C M Wright, A F Auer-Grumbach, M Toscano, A Musumeci, O Valentino, M L Caporali, L Lamperti, C Tallaksen, C M Duffey, P Miller, J Whittaker, R G Baker, M R Jackson, M J Clarke, M P Dhillon, B Czermin, B Stewart, J D Hudson, G Reynier, P Bonneau, D Marques, W Lenaers, G McFarland, R Taylor, R W Turnbull, D M Votruba, M Zeviani, M Carelli, V Bindoff, L A Horvath, R Amati-Bonneau, P Chinnery, P F Producer: 20100413 In: Brain : a journal of neurology vol. 133 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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