Neudle.com: "hypogonadism"

Differential
(Click to cross reference)

acromegaly

acromicria

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adverse drug reaction

aneurysm, intracranial

Angelman syndrome

angiography, cerebral

ataxia telangiectasia

basal ganglia, calcification of

behavior, combative

behavioral disorder

bone marrow transplantation

calcification, intracranial

carcinoma

cardiomyopathy

caries

carotid artery occlusion, intracranial

CAT scan, emission, abnormal

cataracts

celiac disease, adult

celiac disease, childhood

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebrospinal fluid, elevated protein of

cerebrovascular accident

chiasmal syndromes

children

chromophobe adenoma

chromosomal abnormality

chromosome 15

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

coenzyme Q10

coenzyme Q10 deficiency

collateral circulation

complications

contractures, joint

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

cryptorchidism

cultured skin fibroblasts

Cushing's syndrome

degenerative diseases of CNS

dementia

dementia, childhood

demyelinating disease

dermatitis herpetiformis

developmental retardation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

epidemiology of neurology

erectile dysfunction

evoked potentials

exome sequencing

eye movement, disorders of

eyes, sunken

facial appearance, abnormal

failure to thrive

familial

fatty acid, elevated plasma content

feeding disorder

fingers, abnormal

fluorescein angiography

gastrointestinal disease, neurologic complications

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

gonadotropin-releasing hormone

gray hair

growth hormone

growth hormone deficiency

hypogonadism, hypogonadotropic

hypomyelination

hypopigmentation of skin

hypopituitarism

hyposmia

hypothalamus

hypothalamus, damage to

hypothalamus, disturbance of

hypothyroidism

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

Klinefelter's syndrome

magnetic stimulation, brain

monoclonal gammopathy

MRI, contrast enhanced

MRI, disappearing lesion on

MRI, spinal cord

muscle biopsy

muscular dystrophy

myeloma, osteosclerotic

neoplasm, pituitary, incidental

neoplasm, pituitary, treatment of

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic signs

neuronal migration disorder

neuropathy

neuropathy, demyelinating

neuropathy, peripheral

next-generation sequencing

oculopharyngeal muscular dystrophy

photosensitivity, skin

pigmentary retinopathy

pituitary

pituitary stalk

pituitary stalk, lesion of

pituitary, adenoma

pituitary, dysfunction

pituitary, hormones of

pituitary, lesion of

pituitary, microadenoma

Prader-Labhart-Willi syndrome

prenatal diagnosis by amniocentesis

progeria

progressive neurologic disorder

prolactin

prolactin, elevated

prolactinoma

psychomotor retardation

pulmonary infiltrates

radiation therapy, CNS treatment and complications with

sella turcica, enlargement of

sensorineural hearing loss

skin, lesions in neurologic disorders

skull x-ray, abnormal

smell

somatosensory evoked potentials

somatostatin analogue

splenomegaly

steroid therapy, CNS treatment and complications with

temporalis muscle wasting

testicular atrophy

testosterone

testosterone, serum

testosterone, serum, low

third ventricle, wall

thrombocytosis

tongue, protrusion of

treatment of neurologic disorder

vascular endothelial growth factor

visual acuity, decreased

weakness, generalized

X-linked bulbospinal neuronopathy

Showing articles 0 to 30 of 30

Clinical Features, Diagnosis and Management of Klinefelter Syndrome
www.UptoDaate.com, Matsumoto,A.M. & Anawals,B.D., 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016

Extraintestinal Manifestations of Coeliac Disease
Nat Rev Gastroenterol Hepatol 12:561-571, Leffler, D.A.,et al, 2015

Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
NEJM 368:1992-2003, Margolin, D.,et al, 2013

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Prolactinomas
NEJM 362:1219-1226, Klibanski,A., 2010

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

Sarcoidosis: Clinical, Hormonal, and Magnetic Resonance Imaging (MRI) Manifestations of Hypothalamic-Pituitary Disease in 9 Patients and Review of the Literature
Medicine 86:259-268, Bihan,H.,et al, 2007

Late-Onset Cerebellar Ataxia with Hypogonadism and Muscle Coenzyme Q10 Deficiency
Neurol 62:818-820, Gironi,M.,et al, 2004

Prolactinoma
NEJM 349:2035-2041, Schlechte,J.A., 2003

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Diagnosis and Management of Pituitary Tumours
BMJ 308:1087-1091, Levy,A.&Lightman,S.L., 1994

Hypothalamic-Pituitary Dysfunction after Radiation for Brain Tumors
NEJM 328:87-94, Constine,L.S.,et al, 1993

Cortically Evoked Motor Responses in Patients with Xp22. 3-Linked Kallmann's Syndrome and in Female Gene Carriers
Ann Neurol 31:299-304, Danek,A.,et al, 1992

Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
NEJM 326:1752-1755, 17751992., Bick,D.,et al, 1992

Accelerated Aging of the Brain in Werner's Syndrome
Neurol 42:922-924, Kakigi,R.,et al, 1992

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

Neurologic Findings in Men with Isolated Hypogonadotropic Hypogonadism
Neurol 39:223-226, Schwankhau,J.D.,et al, 1989

Syndrome of Cerebellar Ataxia and Hypogonadotrophic Hypogonadism:Evidence for Pituitary Gonadotrophin Deficiency
JNNP 52:407-409, Fox,A.C.K.,et al, 1989

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Isolated CNS Sarcoidosis
JAMA 245:62-63, Cariski,A.T., 1981

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

Prolactin-Secreting Tumors & Hypogonadism in 22 Men
NEJM 299:847-852, Carter,J.N.,et al, 1978

Adrenomyeloneuropathy:A Probable Variant of Adrenoleukodystrophy
Neurol 27:1107-1113, Griffin,J.W.,et al, 1977

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

Showing articles 0 to 30 of 30