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Book Chapter

Spontaneous Closure of Residual Ventricular Septal Defect Following Surgical Repair of Ventricular Septal Defect Complicating Acute Myocardial Infarction

Available to Purchase

Series: Advances in Cardiology
Volume: 27
Published: 26 August 1980
10.1159/000383999
EISBN: 978-3-318-03093-8
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Book Chapter

Thyroid Hormone Cell Membrane Transport Defect

Available to Purchase

Series: Endocrine Development
Volume: 26
Published: 15 September 2014
10.1159/000363158
EISBN: 978-3-318-02721-1
... abnormalities in thyroid function [ 2 , 3 ]. Subsequently it was found that patients described in 1944 with X-chromosome-linked mental retardation by Allan-Herndon-Dudley syndrome also had the thyroid abnormalities and a defect in the MCT8 gene [ 4 ]. MCT8 is expressed in many tissues throughout the body...
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Book Chapter

Model for a Peripheral Signaling Defect in Prader-Willi Syndrome

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Published: 14 July 2003
10.1159/000072590
EISBN: 978-3-318-00970-5
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Book Chapter

Renal Hypouricemia: Classification, Tubular Defect and Clinical Consequences

Available to Purchase

Series: Contributions to Nephrology
Volume: 100
Published: 30 September 1992
10.1159/000421446
EISBN: 978-3-318-03364-9
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Book Chapter

Defect of Opsonophagocytic Function in Burned Patients: Reversal by Transfusion of Normal Plasma or by Cell Wall-Active Antibiotics

Available to Purchase

Series: Antibiotics and Chemotherapy
Volume: 44
Published: 18 November 1991
10.1159/000420306
EISBN: 978-3-318-03219-2
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Book Chapter

Branched-Chain Amino and Keto Acids and Aromatic Amino Acids Profile in Uremia: Nutritional or Metabolic Defect?

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Series: Contributions to Nephrology
Volume: 81
Published: 07 January 1991
10.1159/000418751
EISBN: 978-3-318-03345-8
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Book Chapter

Molecular Mechanism of Temperature-Sensitive Defect of Enterovirus 70

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Published: 14 July 1989
10.1159/000417579
EISBN: 978-3-318-04272-6
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Book Chapter

Dietary Protein Restriction Lessens the Glomerular Permselective Defect in Human Renal Disease1

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Series: Contributions to Nephrology
Volume: 68
Published: 01 December 1988
10.1159/000416507
EISBN: 978-3-318-03332-8
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Book Chapter

Renal Dopamine-1 Defect in Spontaneous Hypertension1

Available to Purchase

Series: Contributions to Nephrology
Volume: 67
Published: 09 November 1988
10.1159/000415377
EISBN: 978-3-318-03331-1
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Book Chapter

Anaerobic Threshold as Detected from Ventilatory and Metabolic Exercise Responses in Patients with Mitochondrial Respiratory Chain Defect

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Series: Advances in Cardiology
Volume: 35
Published: 16 January 1987
10.1159/000413446
EISBN: 978-3-318-03101-0
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Book Chapter

Assessment of the Defect in Distribution and Mixing at Various Lung Volumes

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Series: Progress in Respiratory Research
Volume: 21
Published: 05 August 1986
10.1159/000412914
EISBN: 978-3-318-04124-8
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Book Chapter

Enhanced Miotic Response to Clonidine in Cluster Headache: a Possible Implication for a Central Sympathetic Defect

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Published: 04 December 1985
10.1159/000411500
EISBN: 978-3-318-04938-1
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Book Chapter

Localization of the Defect in Skin Diseases Analyzed in the Human Skin Graft-Nude Mouse Model*

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Series: Current Problems in Dermatology
Volume: 10
Published: 29 April 1981
10.1159/000396285
EISBN: 978-3-318-03447-9
... Abstract Human skin can be grown away from its donor for prolonged periods as grafts on congenitally athymic “nude” mice. This system has been used to analyze the defect in several skin diseases, specifically to localize the site of the defect to the skin itself or to the epidermal or dermal...
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Book Chapter

Comparison between Lung Scans and Pulmonary Angiograms in the Evaluation of the Perfusion Defect in Massive and Submassive Pulmonary Embolism

Available to Purchase

Series: Progress in Respiratory Research
Volume: 13
Published: 22 August 1980
10.1159/000386912
EISBN: 978-3-318-04116-3
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Book Chapter

Hemodialysis Patients with a Unique Mineralizing Defect Unresponsive to 1,25-Dihydroxycholecalciferol: Dialysis Osteomalacic Syndrome

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Series: Contributions to Nephrology
Volume: 18
Published: 07 January 1980
10.1159/000403284
EISBN: 978-3-318-03282-6
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Book Chapter

A Skeletal Mineralizing Defect in Dialysis Patients: a Syndrome Resembling Osteomalacia but Unrelated to Vitamin D

Available to Purchase

Series: Contributions to Nephrology
Volume: 18
Published: 07 January 1980
10.1159/000403285
EISBN: 978-3-318-03282-6
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Book Chapter

Hereditary Coproporphyria: Demonstration of a Genetic Defect in Coproporphyrinogen Metabolism

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Series: Monographs in Human Genetics
Volume: 10
Published: 26 September 1978
10.1159/000401596
EISBN: 978-3-318-04002-9
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Book Chapter

Lactic Acidosis Due to a Defect in the Pyruvate Dehydrogenase Complex: A Possible Brain Pyruvate Dehydrogenase Phosphatase Deficiency

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Series: Monographs in Human Genetics
Volume: 9
Published: 05 September 1978
10.1159/000401601
EISBN: 978-3-318-04001-2
Open the PDF for Lactic Acidosis Due to a Defect in the Pyruvate Dehydrogenase Complex: A Possible Brain Pyruvate Dehydrogenase Phosphatase Deficiency in another window
Book Chapter

Persistent Abnormalities after Repair of Congenital Heart Defects: Ventricular Septal Defect and Tetralogy of Fallot

Available to Purchase

Series: Advances in Cardiology
Volume: 20
Published: 15 March 1977
10.1159/000399859
EISBN: 978-3-318-03086-0
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Book Chapter

Computerized Vectorcardiogram Data in Atrial Septum Primum Defect

Available to Purchase

Series: Advances in Cardiology
Volume: 19
Published: 17 January 1977
10.1159/000399678
EISBN: 978-3-318-03085-3
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