H Jungbluth Selected Research

Failure to Thrive

5/2002

Collagen VI involvement in Ullrich syndrome: a clinical, genetic, and immunohistochemical study.

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H Jungbluth Research Topics

Disease

14	Muscular Diseases (Myopathy) 01/2018 - 01/2000
7	Malignant Hyperthermia 01/2021 - 12/2005
6	Rhabdomyolysis 01/2021 - 07/2013
6	Central Core Myopathy (Central Core Disease) 07/2015 - 07/2002
4	Contracture 04/2019 - 05/2002
4	Minicore Myopathy with External Ophthalmoplegia 07/2015 - 10/2004
4	Congenital Structural Myopathies (Centronuclear Myopathy) 07/2015 - 01/2003
3	Nemaline Myopathies (Nemaline Myopathy) 02/2003 - 01/2001
2	Scoliosis 12/2010 - 05/2002
1	Heat Stress Disorders (Heat Cramp) 05/2023
1	Anxiety Disorders (Anxiety Disorder) 05/2023
1	Fatigue 05/2023
1	Hypersensitivity (Allergy) 01/2021
1	VLCAD deficiency 01/2021
1	Serotonin Syndrome (Syndrome, Serotonin) 12/2020
1	Absent corpus callosum cataract immunodeficiency 01/2018
1	Joint Instability (Joint Laxity) 03/2015
1	Ehlers-Danlos Syndrome (Syndrome, Ehlers-Danlos) 03/2015
1	Marfan Syndrome (Marfan's Syndrome) 03/2015
1	Loeys-Dietz Syndrome 03/2015
1	Myasthenia Gravis 01/2014
1	Neuromuscular Diseases (Neuromuscular Disease) 07/2013
1	Myalgia 07/2013
1	Cytochrome-c Oxidase Deficiency 10/2011
1	Muscle Hypotonia (Hypotonia) 12/2010
1	Respiratory Insufficiency (Respiratory Failure) 12/2010
1	Congenital Myasthenic Syndromes (Myasthenia Gravis, Congenital) 12/2010
1	Disease Progression 04/2009
1	Inflammation (Inflammations) 04/2009
1	Ophthalmoplegia (External Ophthalmoplegia) 12/2005
1	Channelopathies 10/2004
1	Isaacs Syndrome (Neuromyotonia) 10/2004
1	Congenital Abnormalities (Deformity) 10/2004
1	Episodic Ataxia 10/2004
1	Failure to Thrive 05/2002
1	Autosomal Emery-Dreifuss Muscular Dystrophy 02/2002
1	Emery-Dreifuss Muscular Dystrophy (Scapuloperoneal Muscular Dystrophy) 02/2002
1	Hyperekplexia 09/2001
1	Hypoventilation 01/2001
1	Intellectual Disability (Idiocy) 08/2000
1	Walker-Warburg Syndrome 08/2000
1	Muscular Dystrophies (Muscular Dystrophy) 08/2000
1	Neurologic Gait Disorders (Gait, Hemiplegic) 01/2000

Drug/Important Bio-Agent (IBA)

15	Ryanodine Receptor Calcium Release Channel (Ryanodine Receptor)IBA 01/2021 - 07/2002
2	Creatine Kinase (Creatine Phosphokinase)IBA 01/2021 - 01/2000
2	CollagenIBA 03/2015 - 05/2002
2	Selenoproteins (Selenoprotein)IBA 12/2012 - 12/2005
2	myotubularinIBA 05/2012 - 01/2003
2	TropomyosinIBA 12/2010 - 01/2001
2	DNA (Deoxyribonucleic Acid)IBA 08/2003 - 02/2003
2	nebulinIBA 03/2001 - 01/2001
1	4-amino-4'-hydroxylaminodiphenylsulfone (HADS)IBA 05/2023
1	RyanodineIBA 01/2021
1	Antipsychotic Agents (Antipsychotics)IBA 12/2020
1	Proteins (Proteins, Gene)FDA Link 01/2018
1	Nucleic AcidsIBA 01/2018
1	Dantrolene (Dantrium)FDA LinkGeneric 01/2016
1	Neuromuscular Depolarizing AgentsIBA 07/2015
1	Anesthetics (Anesthetic Agents)IBA 07/2015
1	Cholinergic ReceptorsIBA 01/2014
1	Glu Transfer RNAIBA 10/2011
1	Immunoglobulins (Immunoglobulin)IBA 04/2009
1	Potassium Channels (Potassium Channel)IBA 10/2004
1	Albuterol (Salbutamol)FDA LinkGeneric 10/2004
1	PotassiumIBA 10/2004
1	CalciumIBA 02/2003
1	emerinIBA 02/2002
1	Lamin Type A (Lamin A)IBA 02/2002
1	Glycine Receptors (Glycine Receptor)IBA 09/2001
1	Nonsense Codon (Nonsense Mutation)IBA 09/2001
1	Actins (F Actin)IBA 01/2001
1	Laminin (Merosin)IBA 08/2000

Therapy/Procedure

1	Aftercare (After-Treatment) 05/2023
1	Thymectomy 01/2014
1	Noninvasive Ventilation 12/2010