Goebel HH

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References (6)

Title : Human pathology in NCL - Anderson_2013_Biochim.Biophys.Acta_1832_1807
Author(s) : Anderson GW , Goebel HH , Simonati A
Ref : Biochimica & Biophysica Acta , 1832 :1807 , 2013
Abstract : Anderson_2013_Biochim.Biophys.Acta_1832_1807
ESTHER : Anderson_2013_Biochim.Biophys.Acta_1832_1807
PubMedSearch : Anderson_2013_Biochim.Biophys.Acta_1832_1807
PubMedID: 23200925
Gene_locus related to this paper: human-PPT1

Title : Immune-mediated rippling muscle disease with myasthenia gravis: a report of seven patients with long-term follow-up in two - Schoser_2009_Neuromuscul.Disord_19_223
Author(s) : Schoser B , Jacob S , Hilton-Jones D , Muller-Felber W , Kubisch C , Claus D , Goebel HH , Vita G , Vincent A , Toscano A , Van den Bergh P
Ref : Neuromuscular Disorders , 19 :223 , 2009
Abstract : Schoser_2009_Neuromuscul.Disord_19_223
ESTHER : Schoser_2009_Neuromuscul.Disord_19_223
PubMedSearch : Schoser_2009_Neuromuscul.Disord_19_223
PubMedID: 19208478

Title : Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses - Mole_2005_Neurogenetics_6_107
Author(s) : Mole SE , Williams RE , Goebel HH
Ref : Neurogenetics , 6 :107 , 2005
Abstract : Mole_2005_Neurogenetics_6_107
ESTHER : Mole_2005_Neurogenetics_6_107
PubMedSearch : Mole_2005_Neurogenetics_6_107
PubMedID: 15965709

Title : The neuronal ceroid-lipofuscinoses - Goebel_1995_J.Child.Neurol_10_424
Author(s) : Goebel HH
Ref : Journal of Child Neurology , 10 :424 , 1995
Abstract : Goebel_1995_J.Child.Neurol_10_424
ESTHER : Goebel_1995_J.Child.Neurol_10_424
PubMedSearch : Goebel_1995_J.Child.Neurol_10_424
PubMedID: 8576551
Gene_locus related to this paper: human-PPT1

Title : Effects of electrostimulation therapie: enzyme-histological and myometric changes in the denervated musculature -
Author(s) : Stennert E , Boschen C , Gunkel A , Goebel HH
Ref : Eur Arch Otorhinolaryngol , :S37 , 1994
PubMedID: 10774307

Title : Clinical, morphological, and biochemical investigations on a patient with an unusual form of neuronal ceroid-lipofuscinosis - Becker_1979_Eur.J.Pediatr_132_197
Author(s) : Becker K , Goebel HH , Svennerholm L , Wendel U , Bremer HJ
Ref : Eur J Pediatr , 132 :197 , 1979
Abstract : Becker_1979_Eur.J.Pediatr_132_197
ESTHER : Becker_1979_Eur.J.Pediatr_132_197
PubMedSearch : Becker_1979_Eur.J.Pediatr_132_197
PubMedID: 510322
Gene_locus related to this paper: human-PPT1