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Celiac Disease and Autoimmune Thyroid Disease

Clinical medicine & research, 2007-10, Vol.5 (3), p.184-192

2007

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Safety of dual antiplatelet therapy using aspirin and low-dose Prasugrel with platelet reactivity testing in flow diverter treatment of intracranial aneurysms

Interventional neuroradiology, 2023-11, p.15910199231217142-15910199231217142

2023

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Prospective screening for coeliac disease in patients with Graves' hyperthyroidism using anti-gliadin and tissue transglutaminase antibodies

Clinical endocrinology (Oxford), 2005-03, Vol.62 (3), p.303-306

2005

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Acute intermittent porphyria associated with hyperthyroidism

Annals of clinical biochemistry, 2006-09, Vol.43 (Pt 5), p.414-415

2006

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Qualitative Assessment of Brain Anomalies in Adolescents with Mental Retardation

American Journal of Neuroradiology, 2005-11, Vol.26 (10), p.2691-2697

2005

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Management of nodular thyroid disease. The challenge remains identifying which palpable nodules are malignant

BMJ (Online), 2001-08, Vol.323 (7308), p.293

Jones, M K

2001

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Adult Cirrhosis Due to Untreated Congenital Hypopituitarism

Journal of the Royal Society of Medicine, 2005-07, Vol.98 (7), p.316-317

2005

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Management of Papillary and Follicular Thyroid Cancer

Journal of the Royal Society of Medicine, 2002-07, Vol.95 (7), p.325-326

Jones, M Keston

2002

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Completion Thyroidectomy and Thyroglobulin Measurement in the Management of Metastatic Differentiated Thyroid Cancer

Thyroid (New York, N.Y.), 2005-12, Vol.15 (12), p.143-1405

2005

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Hyperthyroidism with Low Thyroid Hormone

Journal of the Royal Society of Medicine, 2003-04, Vol.96 (4), p.185-186

2003

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Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes

Annals of human genetics, 1988-05, Vol.52 (2), p.93-109

1988

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Reversible Pituitary Enlargement in the Syndrome of Resistance to Thyroid Hormone

Thyroid (New York, N.Y.), 1998-08, Vol.8 (8), p.679-682

1998

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Management of nodular thyroid disease

BMJ. British medical journal (International ed.), 2001-08, Vol.323 (7308), p.293

Jones, M Keston

International edition, 2001

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Variation of Sweat Sodium and Chloride with Age in Cystic Fibrosis and Normal Populations: Further Investigations in Equivocal Cases

Annals of clinical biochemistry, 1992-03, Vol.29 (2), p.145-152

1992

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Management of papillary and follicular thyroid cancer

Journal of the Royal Society of Medicine, 2002-07, Vol.95 (7), p.325-326

Jones, M K.

2002

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Substitution of cysteine for glycine at residue 415 of one allele of the α1(I) chain of type I procollagen in type III/IV osteogenesis imperfecta

Journal of medical genetics, 1991, Vol.28 (11), p.757-764

1991

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Exclusion of the α2(I) and α1(III) collagen genes as the mutant loci in a Marfan syndrome family

Journal of medical genetics, 1987, Vol.24 (3), p.148-151

1987

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Triple H Syndrome: A Novel Autoimmune Endocrinopathy Characterized by Dysfunction of the Hippocampus, Hair Follicle, and Hypothalamic-Pituitary-Adrenal Axis

The journal of clinical endocrinology and metabolism, 2000-08, Vol.85 (8), p.2644-2648

2000

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A case of post-operative hypoparathyroidism

Endocrine Abstracts, 2014-04

2014

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Multifocal Fibrosclerosis: A Case of Thyroiditis and Bilateral Lacrimal Gland Involvement

Thyroid (New York, N.Y.), 2001-12, Vol.11 (12), p.1187-1190

2001

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An exclusion map of Marfan syndrome

Journal of medical genetics, 1990-02, Vol.27 (2), p.73-77

1990

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Hyperthyroidism with low thyroid hormone

Journal of the Royal Society of Medicine, 2003-04, Vol.96 (4), p.185-186

2003

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Adult cirrhosis due to untreated congenital hypopituitarism

Journal of the Royal Society of Medicine, 2005-07, Vol.98 (7), p.316-317

Nyunt, A.

2005

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Management of nodular thyroid disease

BMJ, 2001-08, Vol.323 (7308), p.293-294

Jones, M K.

2001

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Three novel mutations in the cystic fibrosis gene detected by chemical cleavage: analysis of variant splicing and a nonsense mutation

Human molecular genetics, 1992-04, Vol.1 (1), p.11-17

1992

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Celiac Disease and Autoimmune Thyroid Disease

Safety of dual antiplatelet therapy using aspirin and low-dose Prasugrel with platelet reactivity testing in flow diverter treatment of intracranial aneurysms

Prospective screening for coeliac disease in patients with Graves' hyperthyroidism using anti-gliadin and tissue transglutaminase antibodies

Acute intermittent porphyria associated with hyperthyroidism

Qualitative Assessment of Brain Anomalies in Adolescents with Mental Retardation

Management of nodular thyroid disease. The challenge remains identifying which palpable nodules are malignant

Adult Cirrhosis Due to Untreated Congenital Hypopituitarism

Management of Papillary and Follicular Thyroid Cancer

Completion Thyroidectomy and Thyroglobulin Measurement in the Management of Metastatic Differentiated Thyroid Cancer

Hyperthyroidism with Low Thyroid Hormone

Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes

Reversible Pituitary Enlargement in the Syndrome of Resistance to Thyroid Hormone

Management of nodular thyroid disease

Variation of Sweat Sodium and Chloride with Age in Cystic Fibrosis and Normal Populations: Further Investigations in Equivocal Cases

Management of papillary and follicular thyroid cancer

Substitution of cysteine for glycine at residue 415 of one allele of the α1(I) chain of type I procollagen in type III/IV osteogenesis imperfecta

Exclusion of the α2(I) and α1(III) collagen genes as the mutant loci in a Marfan syndrome family

Triple H Syndrome: A Novel Autoimmune Endocrinopathy Characterized by Dysfunction of the Hippocampus, Hair Follicle, and Hypothalamic-Pituitary-Adrenal Axis

A case of post-operative hypoparathyroidism

Multifocal Fibrosclerosis: A Case of Thyroiditis and Bilateral Lacrimal Gland Involvement

An exclusion map of Marfan syndrome

Hyperthyroidism with low thyroid hormone

Adult cirrhosis due to untreated congenital hypopituitarism

Management of nodular thyroid disease

Three novel mutations in the cystic fibrosis gene detected by chemical cleavage: analysis of variant splicing and a nonsense mutation

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